Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8626 |
| ensemblid | ENSG00000073282.14 |
| hgncid | 15979 |
| symbol | TP63 |
| name | tumor protein p63 |
| refseq_nuc | NM_001114980.2 |
| refseq_prot | NP_001108452.1 |
| ensembl_nuc | ENST00000354600.10 |
| ensembl_prot | ENSP00000346614.5 |
| mane_status | MANE Plus Clinical |
| chr | chr3 |
| start | 189789659 |
| end | 189897276 |
| strand | + |
| ver | v1.2 |
| region | chr3:189789659-189897276 |
| region5000 | chr3:189784659-189902276 |
| regionname0 | TP63_chr3_189789659_189897276 |
| regionname5000 | TP63_chr3_189784659_189902276 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1758 | 385 | 96 | 74 | 160 | 12 | 41 | TP63_chr3_189784659_189902276 | TP63 | ATGTT others(1753): Show |
chr3 | 189784659 | 189902276 | ||
| a0001c0002 | 0/0 | 1758 | 9 | 0 | 0 | 8 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | ATGTT others(1753): Show |
chr3 | 189784659 | 189902276 | ||
| a0001c0003 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | ATGTT others(1753): Show |
chr3 | 189784659 | 189902276 | ||
| a0001c0004 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | ATGTT others(1753): Show |
chr3 | 189784659 | 189902276 | ||
| a0001c0005 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | ATGTT others(1753): Show |
chr3 | 189784659 | 189902276 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4681 | 109 | 14 | 22 | 64 | 3 | 6 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0002 | 1/1 | 4677 | 91 | 15 | 10 | 49 | 4 | 11 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0003 | 0/0 | 4677 | 52 | 20 | 7 | 14 | 2 | 9 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0004 | 0/0 | 4681 | 18 | 6 | 2 | 7 | 1 | 2 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0005 | 0/0 | 4681 | 14 | 0 | 0 | 13 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0006 | 0/0 | 4677 | 10 | 1 | 2 | 4 | 0 | 3 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0007 | 0/0 | 4677 | 8 | 0 | 7 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0008 | 0/0 | 4679 | 7 | 0 | 5 | 0 | 0 | 2 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4674): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0010 | 0/0 | 4681 | 6 | 6 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0011 | 0/0 | 4681 | 5 | 5 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0012 | 0/0 | 4678 | 5 | 3 | 2 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4673): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0013 | 0/0 | 4681 | 3 | 2 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0014 | 0/0 | 4680 | 3 | 0 | 2 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4675): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0015 | 0/0 | 4680 | 3 | 0 | 3 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4675): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0016 | 0/0 | 4679 | 3 | 1 | 1 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4674): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0017 | 0/0 | 4677 | 3 | 2 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0018 | 0/0 | 4677 | 3 | 3 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0019 | 0/0 | 4676 | 3 | 1 | 2 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4671): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0020 | 0/0 | 4676 | 3 | 0 | 2 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4671): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0021 | 0/0 | 4677 | 3 | 0 | 3 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0022 | 0/0 | 4681 | 2 | 2 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0023 | 0/0 | 4681 | 2 | 2 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0024 | 0/0 | 4678 | 2 | 0 | 1 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4673): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0025 | 0/0 | 4677 | 2 | 2 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0026 | 0/0 | 4677 | 2 | 2 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0027 | 0/0 | 4677 | 2 | 0 | 0 | 2 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0028 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0029 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0030 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0031 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0032 | 0/0 | 4681 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0033 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0034 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0035 | 0/0 | 4681 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0036 | 0/0 | 4681 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0038 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0039 | 0/0 | 4677 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0040 | 0/0 | 4676 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4671): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0041 | 0/0 | 4676 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4671): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0042 | 0/0 | 4677 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0043 | 0/0 | 4677 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0044 | 0/0 | 4677 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0045 | 0/0 | 4677 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0046 | 0/0 | 4677 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0047 | 0/0 | 4677 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0048 | 0/0 | 4677 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0001t0049 | 0/0 | 4677 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0002t0001 | 0/0 | 4681 | 2 | 0 | 0 | 2 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0002t0002 | 0/0 | 4677 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| a0001c0002t0009 | 0/0 | 4681 | 6 | 0 | 0 | 5 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0003t0001 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0003t0004 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0004t0037 | 0/0 | 4681 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4676): Show |
chr3 | 189784659 | 189902276 |
| a0001c0005t0002 | 0/0 | 4677 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | CAGAG others(4672): Show |
chr3 | 189784659 | 189902276 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0346 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0003g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0004g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0005g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0007g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0008g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0010g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0011g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0011g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0011g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0011g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0013g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0013g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0014g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0015g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0015g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0015g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0016g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0016g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0016g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0017g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0018g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0018g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0019g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0019g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0019g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0020g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0020g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0020g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0021g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0021g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0021g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0022g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0022g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0023g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0023g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0024g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0024g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0025g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0026g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0026g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0027g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0027g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0028g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0029g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0030g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0032g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0033g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0034g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0035g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0036g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0038g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0039g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0040g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0041g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0042g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0043g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0044g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0045g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0046g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0047g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0048g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0001t0049g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0002t0009g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0003t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0004t0037g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| a0001c0005t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00099 | hp2 | a0001 | c0001 | t0049 | g0339 | EUR | GBR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | GBR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0343 | EUR | GBR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0149 | EUR | FIN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0283 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0147 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00673 | hp1 | a0001 | c0001 | t0045 | g0188 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0334 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0285 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0319 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0342 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0340 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01070 | hp2 | a0001 | c0001 | t0014 | g0079 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01074 | hp1 | a0001 | c0001 | t0012 | g0019 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0103 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0018 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0323 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01099 | hp2 | a0001 | c0001 | t0021 | g0338 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0146 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01168 | hp2 | a0001 | c0001 | t0021 | g0331 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0148 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0313 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01256 | hp2 | a0001 | c0001 | t0048 | g0217 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01257 | hp1 | a0001 | c0001 | t0043 | g0223 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01261 | hp1 | a0001 | c0001 | t0021 | g0337 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01261 | hp2 | a0001 | c0001 | t0019 | g0174 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01358 | hp1 | a0001 | c0001 | t0019 | g0335 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0289 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0311 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0308 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0219 | EUR | IBS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0332 | EUR | IBS | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0067 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01891 | hp2 | a0001 | c0001 | t0028 | g0310 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0306 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01978 | hp1 | a0001 | c0001 | t0024 | g0317 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01993 | hp1 | a0001 | c0001 | t0020 | g0288 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02015 | hp1 | a0001 | c0001 | t0020 | g0284 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02027 | hp2 | a0001 | c0001 | t0046 | g0169 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02056 | hp1 | a0001 | c0005 | t0002 | g0246 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0361 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0142 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02145 | hp2 | a0001 | c0001 | t0038 | g0033 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02148 | hp2 | a0001 | c0001 | t0014 | g0094 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CDX | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0031 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0307 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02273 | hp1 | a0001 | c0001 | t0020 | g0330 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0387 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0070 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0382 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02523 | hp2 | a0001 | c0002 | t0009 | g0085 | EAS | KHV | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0038 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0012 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0384 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0297 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0347 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0202 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02683 | hp1 | a0001 | c0001 | t0032 | g0290 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0345 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02717 | hp2 | a0001 | c0001 | t0031 | g0096 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02735 | hp1 | a0001 | c0001 | t0014 | g0082 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0395 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0386 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0391 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02895 | hp2 | a0001 | c0001 | t0013 | g0383 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0102 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0390 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02970 | hp1 | a0001 | c0001 | t0022 | g0325 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0093 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03017 | hp1 | a0001 | c0001 | t0024 | g0015 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0385 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0352 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03130 | hp2 | a0001 | c0001 | t0025 | g0041 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03139 | hp2 | a0001 | c0001 | t0029 | g0048 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0098 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0025 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0286 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03239 | hp2 | a0001 | c0002 | t0009 | g0151 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03453 | hp1 | a0001 | c0001 | t0040 | g0348 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0304 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0351 | AFR | ESN | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0392 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0076 | AFR | GWD | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03704 | hp1 | a0001 | c0001 | t0047 | g0235 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0045 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0362 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0324 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0316 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0359 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0341 | SAS | BEB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04199 | hp2 | a0001 | c0001 | t0042 | g0333 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0301 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | STU | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18522 | hp2 | a0001 | c0001 | t0034 | g0280 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | CHB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | CHB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0358 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18939 | hp1 | a0001 | c0002 | t0009 | g0086 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18951 | hp1 | a0001 | c0001 | t0027 | g0239 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0378 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18959 | hp2 | a0001 | c0002 | t0009 | g0084 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18961 | hp1 | a0001 | c0001 | t0036 | g0129 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0373 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18984 | hp2 | a0001 | c0001 | t0035 | g0097 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0377 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18989 | hp1 | a0001 | c0002 | t0009 | g0364 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19006 | hp2 | a0001 | c0001 | t0027 | g0273 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0032 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0309 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0394 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0367 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0380 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19063 | hp2 | a0001 | c0001 | t0039 | g0232 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19082 | hp2 | a0001 | c0004 | t0037 | g0170 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19084 | hp1 | a0001 | c0001 | t0017 | g0160 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19240 | hp1 | a0001 | c0001 | t0026 | g0022 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | YRI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0201 | AFR | ASW | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ASW | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20752 | hp1 | a0001 | c0001 | t0044 | g0176 | EUR | TSI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0287 | EUR | TSI | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0336 | SAS | GIH | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0388 | SAS | GIH | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0296 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02559 | hp1 | a0001 | c0001 | t0033 | g0291 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG02559 | hp2 | a0001 | c0001 | t0030 | g0066 | AFR | ACB | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0393 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0305 | AFR | MSL | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | USA | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | USA | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0036 | AFR | USA | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA21309 | hp1 | a0001 | c0001 | t0041 | g0021 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | LWK | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0346 | REF | REF | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0241 | REF | REF | TP63_chr3_189784659_189902276 | TP63 | chr3 | 189784659 | 189902276 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:189808346 | C | T | 1 | a0001c0003 | 2 | HG03453.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.117C>T | p.Pro39Pro | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/12 | 259/4677 | 117/1761 | 39/586 | chr3 | 189808346 | |||
| chr3:189864285 | C | T | 1 | a0001c0005 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.351C>T | p.Ile117Ile | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/12 | 493/4677 | 351/1761 | 117/586 | chr3 | 189864285 | |||
| chr3:189866774 | C | T | 1 | a0001c0002 | 9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
synonymous_variant | LOW | c.577C>T | p.Leu193Leu | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/12 | 719/4677 | 577/1761 | 193/586 | chr3 | 189866774 | |||
| chr3:189890843 | G | A | 1 | a0001c0004 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.1425G>A | p.Gly475Gly | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/12 | 1567/4677 | 1425/1761 | 475/586 | chr3 | 189890843 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:189789665 | G | C | 4 | a0001c0001t0022 a0001c0001t0028 a0001c0001t0029 others(1): Show |
5 | HG01891.hp2 HG02559.hp2 HG02970.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-136G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/12 | 136 | chr3 | 189789665 | ||||||
| chr3:189789701 | C | T | 2 | a0001c0001t0021 a0001c0001t0049 |
4 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-100C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/12 | 100 | chr3 | 189789701 | ||||||
| chr3:189789729 | C | CAG | 3 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0024 |
12 | HG00741.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-72_-71insAG | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/12 | 71 | chr3 | 189789729 | ||||||
| chr3:189789729 | C | CAGAG | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-72_-71insAGAG | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/12 | 71 | chr3 | 189789729 | ||||||
| chr3:189894547 | C | T | 3 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0024 |
8 | HG00642.hp2 HG01106.hp2 HG01243.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*45C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 45 | chr3 | 189894547 | ||||||
| chr3:189894603 | C | T | 1 | a0001c0001t0048 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 101 | chr3 | 189894603 | ||||||
| chr3:189894937 | C | T | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0004t0037 |
25 | HG01243.hp2 HG01255.hp1 HG02015.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 435 | chr3 | 189894937 | ||||||
| chr3:189894973 | A | T | 1 | a0001c0001t0027 | 2 | NA18951.hp1 NA19006.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 471 | chr3 | 189894973 | ||||||
| chr3:189894989 | G | A | 1 | a0001c0001t0031 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 487 | chr3 | 189894989 | ||||||
| chr3:189895043 | G | A | 9 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0013 others(6): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*541G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 541 | chr3 | 189895043 | ||||||
| chr3:189895129 | T | C | 2 | a0001c0001t0039 a0001c0002t0009 |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*627T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 627 | chr3 | 189895129 | ||||||
| chr3:189895140 | C | G | 2 | a0001c0001t0010 a0001c0001t0026 |
8 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*638C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 638 | chr3 | 189895140 | ||||||
| chr3:189895322 | C | T | 1 | a0001c0004t0037 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 820 | chr3 | 189895322 | ||||||
| chr3:189895356 | A | G | 1 | a0001c0001t0019 | 3 | HG01261.hp2 HG01358.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*854A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 854 | chr3 | 189895356 | ||||||
| chr3:189895454 | A | G | 1 | a0001c0001t0036 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 952 | chr3 | 189895454 | ||||||
| chr3:189895845 | T | C | 1 | a0001c0001t0023 | 2 | HG02647.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1343T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1343 | chr3 | 189895845 | ||||||
| chr3:189895888 | T | C | 3 | a0001c0001t0018 a0001c0001t0029 a0001c0001t0034 |
5 | HG02257.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1386T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1386 | chr3 | 189895888 | ||||||
| chr3:189895966 | G | T | 1 | a0001c0001t0047 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1464 | chr3 | 189895966 | ||||||
| chr3:189896345 | T | TA | 1 | a0001c0001t0012 | 5 | HG01074.hp1 HG01081.hp2 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1844dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1845 | INFO_REALIGN_3_PRIME | chr3 | 189896345 | |||||
| chr3:189896401 | G | T | 1 | a0001c0001t0046 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1899G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1899 | chr3 | 189896401 | ||||||
| chr3:189896460 | T | A | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1958T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1958 | chr3 | 189896460 | ||||||
| chr3:189896483 | A | G | 1 | a0001c0001t0045 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 1981 | chr3 | 189896483 | ||||||
| chr3:189896518 | A | G | 1 | a0001c0001t0013 | 3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2016A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2016 | chr3 | 189896518 | ||||||
| chr3:189896625 | C | T | 1 | a0001c0001t0044 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2123C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2123 | chr3 | 189896625 | ||||||
| chr3:189896641 | G | A | 1 | a0001c0001t0025 | 2 | HG03130.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2139G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2139 | chr3 | 189896641 | ||||||
| chr3:189896718 | G | A | 2 | a0001c0001t0007 a0001c0001t0032 |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2216G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2216 | chr3 | 189896718 | ||||||
| chr3:189896786 | C | T | 1 | a0001c0001t0035 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2284C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2284 | chr3 | 189896786 | ||||||
| chr3:189896813 | G | T | 1 | a0001c0001t0043 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2311G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2311 | chr3 | 189896813 | ||||||
| chr3:189896847 | C | T | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 others(6): Show |
81 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2345C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2345 | chr3 | 189896847 | ||||||
| chr3:189896928 | C | T | 1 | a0001c0001t0042 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2426C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2426 | chr3 | 189896928 | ||||||
| chr3:189896979 | T | G | 1 | a0001c0002t0009 | 6 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2477T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2477 | chr3 | 189896979 | ||||||
| chr3:189897039 | AT | A | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0024 others(1): Show |
9 | HG00642.hp2 HG01106.hp2 HG01243.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2544delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2544 | INFO_REALIGN_3_PRIME | chr3 | 189897039 | |||||
| chr3:189897137 | CA | C | 3 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0041 |
7 | HG01070.hp2 HG01261.hp2 HG01358.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2636delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2636 | chr3 | 189897137 | ||||||
| chr3:189897188 | T | C | 2 | a0001c0001t0033 a0001c0001t0038 |
2 | HG02145.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2686T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 12/12 | 2686 | chr3 | 189897188 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:189789912 | C | G | 1 | a0001c0001t0003g0395 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.42+70C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189789912 | |||||||
| chr3:189790077 | A | G | 5 | a0001c0001t0001g0394 a0001c0001t0004g0392 a0001c0001t0004g0393 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+235A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790077 | |||||||
| chr3:189790290 | A | G | 1 | a0001c0001t0001g0389 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.42+448A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790290 | |||||||
| chr3:189790291 | T | G | 41 | a0001c0001t0001g0043 a0001c0001t0002g0009 a0001c0001t0002g0016 others(38): Show |
41 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.42+449T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790291 | |||||||
| chr3:189790513 | A | G | 90 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(87): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.42+671A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790513 | |||||||
| chr3:189790558 | T | C | 93 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(90): Show |
95 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.42+716T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790558 | |||||||
| chr3:189790584 | T | TA | 89 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(86): Show |
91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.42+753dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189790584 | ||||||
| chr3:189790682 | G | A | 90 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(87): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.42+840G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790682 | |||||||
| chr3:189790777 | T | C | 90 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(87): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.42+935T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790777 | |||||||
| chr3:189790829 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0002g0040 a0001c0001t0002g0042 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+987C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189790829 | |||||||
| chr3:189791010 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.42+1168C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791010 | |||||||
| chr3:189791145 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.42+1303G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791145 | |||||||
| chr3:189791661 | T | C | 1 | a0001c0001t0029g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+1819T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791661 | |||||||
| chr3:189791806 | T | C | 18 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(15): Show |
18 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+1964T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791806 | |||||||
| chr3:189791897 | T | G | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(2): Show |
5 | HG01243.hp2 HG01346.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+2055T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791897 | |||||||
| chr3:189791908 | T | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.42+2066T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791908 | |||||||
| chr3:189791962 | G | C | 2 | a0001c0001t0003g0011 a0001c0001t0012g0010 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.42+2120G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189791962 | |||||||
| chr3:189792044 | A | G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+2202A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792044 | |||||||
| chr3:189792227 | A | G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+2385A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792227 | |||||||
| chr3:189792240 | C | G | 6 | a0001c0001t0001g0384 a0001c0001t0001g0385 a0001c0001t0010g0387 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+2398C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792240 | |||||||
| chr3:189792274 | C | T | 21 | a0001c0001t0001g0298 a0001c0001t0002g0282 a0001c0001t0002g0287 others(18): Show |
22 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.42+2432C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792274 | |||||||
| chr3:189792531 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.42+2689G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792531 | |||||||
| chr3:189792681 | A | G | 24 | a0001c0001t0001g0360 a0001c0001t0001g0363 a0001c0001t0001g0365 others(21): Show |
24 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+2839A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792681 | |||||||
| chr3:189792726 | A | G | 1 | a0001c0001t0008g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.42+2884A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792726 | |||||||
| chr3:189792782 | T | C | 5 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0002g0302 others(2): Show |
5 | HG03491.hp2 HG03492.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+2940T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792782 | |||||||
| chr3:189792801 | T | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0002t0001g0061 |
3 | NA18965.hp1 NA18983.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.42+2959T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792801 | |||||||
| chr3:189792983 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.42+3141T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189792983 | |||||||
| chr3:189793273 | G | C | 3 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0016g0307 |
3 | HG01496.hp1 HG01975.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.42+3431G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793273 | |||||||
| chr3:189793285 | T | G | 1 | a0001c0001t0034g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.42+3443T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793285 | |||||||
| chr3:189793326 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.42+3484C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793326 | |||||||
| chr3:189793355 | T | A | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+3513T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793355 | |||||||
| chr3:189793498 | A | G | 31 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(28): Show |
31 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.42+3656A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793498 | |||||||
| chr3:189793502 | A | G | 23 | a0001c0001t0002g0332 a0001c0001t0002g0336 a0001c0001t0002g0343 others(20): Show |
25 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.42+3660A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793502 | |||||||
| chr3:189793575 | G | A | 312 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.42+3733G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793575 | |||||||
| chr3:189793620 | T | A | 6 | a0001c0001t0001g0394 a0001c0001t0004g0392 a0001c0001t0004g0393 others(3): Show |
6 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+3778T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793620 | |||||||
| chr3:189793686 | A | T | 16 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.42+3844A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793686 | |||||||
| chr3:189793832 | G | A | 4 | a0001c0001t0002g0069 a0001c0001t0003g0068 a0001c0001t0010g0067 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+3990G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189793832 | |||||||
| chr3:189794178 | G | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0004g0207 |
3 | HG00544.hp2 NA18747.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.42+4336G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189794178 | |||||||
| chr3:189794336 | TAC | T | 67 | a0001c0001t0001g0064 a0001c0001t0001g0145 a0001c0001t0001g0152 others(64): Show |
67 | HG00280.hp2 HG00609.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.42+4496_42+4497del others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189794336 | ||||||
| chr3:189794344 | A | G | 35 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(32): Show |
35 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.42+4502A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189794344 | |||||||
| chr3:189794424 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.42+4582A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189794424 | |||||||
| chr3:189794544 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.42+4702G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189794544 | |||||||
| chr3:189794818 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.42+4976A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189794818 | |||||||
| chr3:189795030 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.42+5188A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795030 | |||||||
| chr3:189795294 | C | G | 1 | a0001c0002t0009g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.42+5452C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795294 | |||||||
| chr3:189795381 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0005g0361 |
2 | HG00438.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.42+5539G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795381 | |||||||
| chr3:189795518 | T | G | 1 | a0001c0001t0003g0362 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.42+5676T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795518 | |||||||
| chr3:189795533 | C | G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+5691C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795533 | |||||||
| chr3:189795535 | T | G | 3 | a0001c0001t0001g0363 a0001c0001t0001g0365 a0001c0002t0009g0364 |
3 | NA18975.hp1 NA18989.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.42+5693T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795535 | |||||||
| chr3:189795548 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.42+5706G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795548 | |||||||
| chr3:189795971 | C | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.42+6129C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189795971 | |||||||
| chr3:189796172 | T | C | 13 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+6330T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796172 | |||||||
| chr3:189796238 | T | A | 1 | a0001c0001t0003g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.42+6396T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796238 | |||||||
| chr3:189796245 | A | G | 1 | a0001c0001t0022g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.42+6403A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796245 | |||||||
| chr3:189796258 | A | G | 54 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.42+6416A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796258 | |||||||
| chr3:189796450 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0013g0201 a0001c0001t0023g0202 |
3 | HG02647.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.42+6608C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796450 | |||||||
| chr3:189796453 | G | A | 8 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0002g0302 others(5): Show |
8 | HG01891.hp2 HG02970.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+6611G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796453 | |||||||
| chr3:189796510 | A | G | 7 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+6668A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796510 | |||||||
| chr3:189796543 | C | CT | 7 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+6709dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189796543 | ||||||
| chr3:189796689 | A | C | 12 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+6847A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796689 | |||||||
| chr3:189796773 | A | G | 6 | a0001c0001t0001g0384 a0001c0001t0001g0385 a0001c0001t0010g0387 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+6931A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796773 | |||||||
| chr3:189796889 | G | A | 6 | a0001c0001t0001g0394 a0001c0001t0004g0392 a0001c0001t0004g0393 others(3): Show |
6 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+7047G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189796889 | |||||||
| chr3:189797238 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0034g0280 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42+7396C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189797238 | |||||||
| chr3:189797612 | G | A | 1 | a0001c0001t0012g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.42+7770G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189797612 | |||||||
| chr3:189797714 | G | A | 18 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.42+7872G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189797714 | |||||||
| chr3:189797778 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.42+7936G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189797778 | |||||||
| chr3:189798021 | C | T | 3 | a0001c0001t0022g0309 a0001c0001t0022g0325 a0001c0001t0028g0310 |
3 | HG01891.hp2 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.42+8179C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798021 | |||||||
| chr3:189798183 | T | C | 1 | a0001c0001t0003g0211 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.42+8341T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798183 | |||||||
| chr3:189798194 | T | C | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.42+8352T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798194 | |||||||
| chr3:189798198 | A | G | 18 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.42+8356A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798198 | |||||||
| chr3:189798244 | G | A | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | NA19010.hp2 NA19057.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.42+8402G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798244 | |||||||
| chr3:189798384 | A | T | 1 | a0001c0001t0002g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.42+8542A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798384 | |||||||
| chr3:189798396 | T | A | 1 | a0001c0001t0011g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.42+8554T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798396 | |||||||
| chr3:189798644 | T | G | 2 | a0001c0001t0002g0282 a0001c0001t0003g0281 |
2 | HG00738.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.42+8802T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798644 | |||||||
| chr3:189798652 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42+8810C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798652 | |||||||
| chr3:189798791 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42+8949C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798791 | |||||||
| chr3:189798797 | G | C | 21 | a0001c0001t0001g0360 a0001c0001t0001g0363 a0001c0001t0001g0365 others(18): Show |
21 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.42+8955G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189798797 | |||||||
| chr3:189799072 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-9200T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799072 | |||||||
| chr3:189799308 | G | A | 18 | a0001c0001t0002g0332 a0001c0001t0002g0336 a0001c0001t0002g0343 others(15): Show |
20 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-8964G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799308 | |||||||
| chr3:189799315 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8957G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799315 | |||||||
| chr3:189799334 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8938A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799334 | |||||||
| chr3:189799383 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.43-8889C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799383 | |||||||
| chr3:189799475 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8797T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799475 | |||||||
| chr3:189799565 | A | G | 1 | a0001c0001t0003g0358 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-8707A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799565 | |||||||
| chr3:189799618 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8654T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799618 | |||||||
| chr3:189799993 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8279T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189799993 | |||||||
| chr3:189800089 | T | C | 18 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.43-8183T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800089 | |||||||
| chr3:189800158 | G | T | 1 | a0001c0001t0002g0278 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43-8114G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800158 | |||||||
| chr3:189800164 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.43-8108C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800164 | |||||||
| chr3:189800475 | T | TA | 108 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.43-7783dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189800475 | ||||||
| chr3:189800488 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-7784A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800488 | |||||||
| chr3:189800490 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-7782G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800490 | |||||||
| chr3:189800509 | A | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0197 a0001c0002t0001g0198 |
3 | NA18945.hp2 NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.43-7763A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800509 | |||||||
| chr3:189800611 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-7661G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800611 | |||||||
| chr3:189800741 | A | C | 1 | a0001c0001t0003g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43-7531A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800741 | |||||||
| chr3:189800914 | T | C | 1 | a0001c0001t0008g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.43-7358T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189800914 | |||||||
| chr3:189801094 | A | C | 5 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0008g0324 others(2): Show |
5 | HG01496.hp1 HG01975.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-7178A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801094 | |||||||
| chr3:189801118 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-7154C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801118 | |||||||
| chr3:189801142 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-7130G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801142 | |||||||
| chr3:189801333 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.43-6939G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801333 | |||||||
| chr3:189801629 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-6643A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801629 | |||||||
| chr3:189801768 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-6504A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801768 | |||||||
| chr3:189801820 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43-6452C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801820 | |||||||
| chr3:189801971 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43-6301C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801971 | |||||||
| chr3:189801985 | G | T | 1 | a0001c0001t0003g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.43-6287G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801985 | |||||||
| chr3:189801999 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-6273C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189801999 | |||||||
| chr3:189802010 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.43-6262C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802010 | |||||||
| chr3:189802300 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5972C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802300 | |||||||
| chr3:189802303 | C | T | 1 | a0001c0003t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-5969C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802303 | |||||||
| chr3:189802397 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5875G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802397 | |||||||
| chr3:189802441 | G | A | 1 | a0001c0001t0035g0097 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.43-5831G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802441 | |||||||
| chr3:189802446 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.43-5826A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802446 | |||||||
| chr3:189802527 | A | G | 28 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(25): Show |
28 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.43-5745A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802527 | |||||||
| chr3:189802617 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5655A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802617 | |||||||
| chr3:189802648 | A | G | 18 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.43-5624A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802648 | |||||||
| chr3:189802716 | G | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0010g0098 |
3 | HG00639.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43-5556G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802716 | |||||||
| chr3:189802727 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5545C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802727 | |||||||
| chr3:189802753 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5519C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802753 | |||||||
| chr3:189802780 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5492T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802780 | |||||||
| chr3:189802807 | T | C | 10 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0002g0218 others(7): Show |
10 | HG00280.hp1 HG00741.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.43-5465T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802807 | |||||||
| chr3:189802839 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5433C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802839 | |||||||
| chr3:189802856 | A | T | 2 | a0001c0001t0001g0138 a0001c0001t0005g0139 |
2 | NA18947.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.43-5416A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802856 | |||||||
| chr3:189802879 | C | T | 7 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-5393C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802879 | |||||||
| chr3:189802882 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-5390C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189802882 | |||||||
| chr3:189803022 | G | A | 78 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(75): Show |
78 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.43-5250G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803022 | |||||||
| chr3:189803089 | G | A | 1 | a0001c0001t0034g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.43-5183G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803089 | |||||||
| chr3:189803108 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.43-5164G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803108 | |||||||
| chr3:189803163 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.43-5109T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803163 | |||||||
| chr3:189803403 | A | G | 19 | a0001c0001t0001g0299 a0001c0001t0002g0332 a0001c0001t0002g0336 others(16): Show |
21 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.43-4869A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803403 | |||||||
| chr3:189803433 | T | C | 1 | a0001c0001t0020g0330 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.43-4839T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803433 | |||||||
| chr3:189803451 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4821G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803451 | |||||||
| chr3:189803530 | T | G | 19 | a0001c0001t0001g0299 a0001c0001t0002g0332 a0001c0001t0002g0336 others(16): Show |
21 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.43-4742T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803530 | |||||||
| chr3:189803583 | G | T | 111 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(108): Show |
111 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.43-4689G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803583 | |||||||
| chr3:189803584 | C | T | 111 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(108): Show |
111 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.43-4688C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803584 | |||||||
| chr3:189803649 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4623T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803649 | |||||||
| chr3:189803658 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4614C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803658 | |||||||
| chr3:189803788 | C | A | 5 | a0001c0001t0002g0349 a0001c0001t0002g0350 a0001c0001t0003g0347 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-4484C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803788 | |||||||
| chr3:189803853 | G | A | 7 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0002g0302 others(4): Show |
7 | HG01891.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-4419G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803853 | |||||||
| chr3:189803878 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4394G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189803878 | |||||||
| chr3:189804007 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4265A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804007 | |||||||
| chr3:189804069 | C | T | 1 | a0001c0001t0002g0345 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.43-4203C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804069 | |||||||
| chr3:189804109 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4163A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804109 | |||||||
| chr3:189804183 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-4089G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804183 | |||||||
| chr3:189804264 | G | A | 6 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(3): Show |
6 | HG00597.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-4008G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804264 | |||||||
| chr3:189804341 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.43-3931C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804341 | |||||||
| chr3:189804351 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.43-3921A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804351 | |||||||
| chr3:189804469 | A | G | 108 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.43-3803A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804469 | |||||||
| chr3:189804497 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3775A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804497 | |||||||
| chr3:189804529 | T | G | 2 | a0001c0001t0002g0233 a0001c0001t0002g0277 |
2 | HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.43-3743T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804529 | |||||||
| chr3:189804561 | G | C | 4 | a0001c0001t0004g0149 a0001c0001t0015g0146 a0001c0001t0015g0147 others(1): Show |
4 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-3711G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804561 | |||||||
| chr3:189804627 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3645T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804627 | |||||||
| chr3:189804710 | A | C | 1 | a0001c0001t0002g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-3562A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804710 | |||||||
| chr3:189804729 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43-3543G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804729 | |||||||
| chr3:189804729 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3543G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189804729 | |||||||
| chr3:189805063 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0002t0001g0061 |
3 | NA18965.hp1 NA18983.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.43-3209C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805063 | |||||||
| chr3:189805176 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3096A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805176 | |||||||
| chr3:189805199 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3073C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805199 | |||||||
| chr3:189805208 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-3064C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805208 | |||||||
| chr3:189805267 | A | G | 2 | a0001c0001t0008g0311 a0001c0001t0008g0323 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.43-3005A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805267 | |||||||
| chr3:189805306 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0191 |
3 | HG00609.hp1 HG00673.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.43-2966A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805306 | |||||||
| chr3:189805313 | T | C | 1 | a0001c0002t0009g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.43-2959T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805313 | |||||||
| chr3:189805506 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-2766G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805506 | |||||||
| chr3:189805590 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.43-2682G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805590 | |||||||
| chr3:189805614 | G | A | 29 | a0001c0001t0001g0138 a0001c0001t0001g0152 a0001c0001t0001g0153 others(26): Show |
29 | HG00609.hp1 HG00673.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.43-2658G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805614 | |||||||
| chr3:189805633 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-2639G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805633 | |||||||
| chr3:189805646 | C | T | 1 | a0001c0001t0031g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.43-2626C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805646 | |||||||
| chr3:189805757 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-2515G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805757 | |||||||
| chr3:189805962 | G | A | 7 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0002g0302 others(4): Show |
7 | HG01891.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-2310G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189805962 | |||||||
| chr3:189806040 | C | CT | 160 | a0001c0001t0001g0043 a0001c0001t0001g0062 a0001c0001t0001g0063 others(157): Show |
161 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.43-2205dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189806040 | ||||||
| chr3:189806040 | C | CTT | 41 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0001t0001g0190 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.43-2206_43-2205dup others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189806040 | ||||||
| chr3:189806040 | C | CTTT | 8 | a0001c0001t0001g0365 a0001c0001t0001g0379 a0001c0001t0001g0381 others(5): Show |
8 | HG02280.hp1 HG02615.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-2207_43-2205dup others(3): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189806040 | ||||||
| chr3:189806040 | CT | C | 18 | a0001c0001t0001g0058 a0001c0001t0001g0141 a0001c0001t0001g0312 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-2205delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189806040 | ||||||
| chr3:189806040 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0002g0302 others(2): Show |
5 | HG03491.hp2 HG03492.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-2214_43-2205del others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 189806040 | ||||||
| chr3:189806049 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0048g0217 |
2 | HG01074.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.43-2223T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806049 | |||||||
| chr3:189806102 | C | T | 7 | a0001c0001t0001g0195 a0001c0001t0002g0268 a0001c0001t0002g0269 others(4): Show |
7 | HG00621.hp2 NA18952.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-2170C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806102 | |||||||
| chr3:189806155 | C | G | 1 | a0001c0001t0010g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.43-2117C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806155 | |||||||
| chr3:189806165 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.43-2107C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806165 | |||||||
| chr3:189806230 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.43-2042A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806230 | |||||||
| chr3:189806308 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG04204.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.43-1964G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806308 | |||||||
| chr3:189806486 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-1786G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806486 | |||||||
| chr3:189806679 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-1593A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806679 | |||||||
| chr3:189806780 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43-1492G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189806780 | |||||||
| chr3:189807125 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-1147C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807125 | |||||||
| chr3:189807147 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-1125G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807147 | |||||||
| chr3:189807220 | C | T | 4 | a0001c0001t0002g0343 a0001c0001t0003g0341 a0001c0001t0003g0378 others(1): Show |
4 | HG00140.hp2 HG01069.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1052C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807220 | |||||||
| chr3:189807312 | G | A | 13 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(10): Show |
13 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.43-960G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807312 | |||||||
| chr3:189807464 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-808G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807464 | |||||||
| chr3:189807482 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.43-790C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807482 | |||||||
| chr3:189807577 | A | T | 8 | a0001c0001t0003g0318 a0001c0001t0008g0306 a0001c0001t0008g0308 others(5): Show |
8 | HG00741.hp1 HG01496.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-695A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189807577 | |||||||
| chr3:189808004 | A | G | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-268A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808004 | |||||||
| chr3:189808136 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0012g0010 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.43-136G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808136 | |||||||
| chr3:189808191 | A | G | 1 | a0001c0001t0010g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.43-81A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808191 | |||||||
| chr3:189808196 | C | A | 4 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0008g0324 others(1): Show |
4 | HG01496.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-76C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808196 | |||||||
| chr3:189808197 | C | T | 4 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0008g0324 others(1): Show |
4 | HG01496.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-75C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808197 | |||||||
| chr3:189808238 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-34C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808238 | |||||||
| chr3:189808239 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43-33G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 1/11 | chr3 | 189808239 | |||||||
| chr3:189808684 | T | A | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+158T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189808684 | |||||||
| chr3:189808995 | A | G | 1 | a0001c0001t0020g0288 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.297+469A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189808995 | |||||||
| chr3:189808996 | TGAAG | T | 4 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0008g0324 others(1): Show |
4 | HG01496.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+477_297+480del others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189808996 | ||||||
| chr3:189809080 | TATTTATA | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0004g0095 |
3 | HG01109.hp2 HG01175.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.297+561_297+567del others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189809080 | ||||||
| chr3:189809230 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+704A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809230 | |||||||
| chr3:189809331 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+805T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809331 | |||||||
| chr3:189809357 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+831T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809357 | |||||||
| chr3:189809388 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0197 a0001c0002t0001g0198 |
3 | NA18945.hp2 NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.297+862T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809388 | |||||||
| chr3:189809388 | T | C | 259 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.297+862T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809388 | |||||||
| chr3:189809417 | A | G | 1 | a0001c0001t0005g0361 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.297+891A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809417 | |||||||
| chr3:189809483 | TTCAAGAC others(29): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+995_297+1030de others(37): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189809483 | ||||||
| chr3:189809845 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+1319T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189809845 | |||||||
| chr3:189810138 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+1612A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810138 | |||||||
| chr3:189810142 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+1616A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810142 | |||||||
| chr3:189810300 | C | T | 5 | a0001c0001t0002g0349 a0001c0001t0002g0350 a0001c0001t0003g0347 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1774C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810300 | |||||||
| chr3:189810379 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.297+1853G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810379 | |||||||
| chr3:189810455 | G | A | 1 | a0001c0001t0012g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+1929G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810455 | |||||||
| chr3:189810693 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.297+2167T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810693 | |||||||
| chr3:189810716 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+2190C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810716 | |||||||
| chr3:189810804 | T | C | 20 | a0001c0001t0002g0225 a0001c0001t0002g0234 a0001c0001t0002g0332 others(17): Show |
22 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.297+2278T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810804 | |||||||
| chr3:189810859 | C | CAAA | 36 | a0001c0001t0001g0299 a0001c0001t0001g0312 a0001c0001t0001g0314 others(33): Show |
38 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.297+2347_297+2349d others(5): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189810859 | ||||||
| chr3:189810859 | C | CAAAA | 96 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(93): Show |
97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.297+2346_297+2349d others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189810859 | ||||||
| chr3:189810989 | T | C | 136 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.297+2463T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189810989 | |||||||
| chr3:189811063 | C | A | 157 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(154): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.297+2537C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811063 | |||||||
| chr3:189811122 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+2596A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811122 | |||||||
| chr3:189811201 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.297+2675A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811201 | |||||||
| chr3:189811211 | A | G | 19 | a0001c0001t0001g0388 a0001c0001t0001g0394 a0001c0001t0002g0300 others(16): Show |
19 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+2685A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811211 | |||||||
| chr3:189811266 | G | A | 269 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.297+2740G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811266 | |||||||
| chr3:189811267 | T | C | 104 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(101): Show |
104 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.297+2741T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811267 | |||||||
| chr3:189811383 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+2857C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811383 | |||||||
| chr3:189811408 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.297+2882A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811408 | |||||||
| chr3:189811447 | C | A | 109 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(106): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.297+2921C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811447 | |||||||
| chr3:189811474 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.297+2948C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811474 | |||||||
| chr3:189811491 | T | A | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0024 others(15): Show |
18 | HG01243.hp2 HG01346.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.297+2965T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811491 | |||||||
| chr3:189811744 | G | A | 17 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(14): Show |
17 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+3218G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811744 | |||||||
| chr3:189811798 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.297+3272A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189811798 | |||||||
| chr3:189812020 | C | T | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+3494C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812020 | |||||||
| chr3:189812176 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.297+3650C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812176 | |||||||
| chr3:189812180 | C | T | 102 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(99): Show |
102 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.297+3654C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812180 | |||||||
| chr3:189812258 | C | T | 1 | a0001c0002t0009g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+3732C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812258 | |||||||
| chr3:189812294 | G | C | 6 | a0001c0001t0001g0354 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+3768G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812294 | |||||||
| chr3:189812422 | C | T | 102 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(99): Show |
102 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.297+3896C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812422 | |||||||
| chr3:189812509 | T | C | 1 | a0001c0001t0034g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.297+3983T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812509 | |||||||
| chr3:189812641 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0184 a0001c0001t0001g0190 |
3 | NA18953.hp2 NA18962.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.297+4115A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812641 | |||||||
| chr3:189812878 | G | A | 1 | a0001c0001t0002g0332 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.297+4352G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812878 | |||||||
| chr3:189812924 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.297+4398G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812924 | |||||||
| chr3:189812945 | A | G | 78 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(75): Show |
78 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.297+4419A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189812945 | |||||||
| chr3:189813047 | G | A | 3 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0004g0301 |
3 | HG03834.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.297+4521G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813047 | |||||||
| chr3:189813110 | A | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.297+4584A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813110 | |||||||
| chr3:189813111 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+4585C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813111 | |||||||
| chr3:189813300 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.297+4774C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813300 | |||||||
| chr3:189813433 | G | GT | 14 | a0001c0001t0001g0388 a0001c0001t0001g0394 a0001c0001t0002g0300 others(11): Show |
14 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+4910dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189813433 | ||||||
| chr3:189813479 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+4953G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813479 | |||||||
| chr3:189813545 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.297+5019A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813545 | |||||||
| chr3:189813569 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+5043G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813569 | |||||||
| chr3:189813594 | T | TG | 144 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.297+5069dupG | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189813594 | ||||||
| chr3:189813595 | G | GGT | 3 | a0001c0001t0001g0054 a0001c0001t0002g0345 a0001c0001t0017g0032 |
3 | HG01934.hp1 HG02683.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.297+5069_297+5070i others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813595 | |||||||
| chr3:189813707 | C | A | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(2): Show |
5 | HG01243.hp2 HG01346.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+5181C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813707 | |||||||
| chr3:189813737 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.297+5211T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813737 | |||||||
| chr3:189813764 | A | C | 3 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0004g0301 |
3 | HG03834.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.297+5238A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813764 | |||||||
| chr3:189813792 | A | G | 3 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0004g0301 |
3 | HG03834.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.297+5266A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813792 | |||||||
| chr3:189813943 | T | TGCCA | 4 | a0001c0001t0008g0306 a0001c0001t0008g0308 a0001c0001t0008g0324 others(1): Show |
4 | HG01496.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+5420_297+5423d others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189813943 | ||||||
| chr3:189813952 | C | T | 2 | a0001c0001t0001g0394 a0001c0001t0004g0393 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.297+5426C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189813952 | |||||||
| chr3:189814102 | C | T | 2 | a0001c0001t0022g0309 a0001c0001t0028g0310 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.297+5576C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814102 | |||||||
| chr3:189814122 | C | T | 11 | a0001c0001t0002g0282 a0001c0001t0002g0287 a0001c0001t0003g0001 others(8): Show |
12 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+5596C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814122 | |||||||
| chr3:189814224 | G | A | 3 | a0001c0001t0001g0388 a0001c0001t0002g0300 a0001c0001t0004g0301 |
3 | HG03834.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.297+5698G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814224 | |||||||
| chr3:189814305 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.297+5779G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814305 | |||||||
| chr3:189814382 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.297+5856T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814382 | |||||||
| chr3:189814474 | A | G | 5 | a0001c0001t0002g0349 a0001c0001t0002g0350 a0001c0001t0003g0347 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+5948A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814474 | |||||||
| chr3:189814476 | A | C | 9 | a0001c0001t0002g0069 a0001c0001t0003g0020 a0001c0001t0003g0068 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+5950A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814476 | |||||||
| chr3:189814614 | G | T | 1 | a0001c0001t0002g0231 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.297+6088G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814614 | |||||||
| chr3:189814855 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.297+6329C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814855 | |||||||
| chr3:189814862 | T | C | 12 | a0001c0001t0001g0394 a0001c0001t0002g0069 a0001c0001t0003g0020 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+6336T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814862 | |||||||
| chr3:189814898 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.297+6372A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189814898 | |||||||
| chr3:189815000 | T | A | 3 | a0001c0001t0003g0014 a0001c0001t0003g0362 a0001c0001t0024g0015 |
3 | HG02602.hp2 HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.297+6474T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815000 | |||||||
| chr3:189815002 | CAA | C | 206 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(203): Show |
207 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.297+6478_297+6479d others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189815002 | ||||||
| chr3:189815027 | G | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0200 |
2 | HG01069.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.297+6501G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815027 | |||||||
| chr3:189815053 | A | G | 31 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(28): Show |
31 | HG00099.hp1 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.297+6527A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815053 | |||||||
| chr3:189815079 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+6553C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815079 | |||||||
| chr3:189815089 | T | C | 43 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(40): Show |
44 | HG00609.hp2 HG00733.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.297+6563T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815089 | |||||||
| chr3:189815185 | A | AT | 17 | a0001c0001t0001g0388 a0001c0001t0001g0394 a0001c0001t0002g0069 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+6668dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189815185 | ||||||
| chr3:189815185 | A | ATT | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(7): Show |
10 | HG00099.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+6667_297+6668d others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189815185 | ||||||
| chr3:189815235 | A | G | 61 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0190 others(58): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.297+6709A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815235 | |||||||
| chr3:189815280 | A | G | 4 | a0001c0001t0002g0350 a0001c0001t0003g0347 a0001c0001t0003g0351 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+6754A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815280 | |||||||
| chr3:189815295 | T | C | 6 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0001g0312 others(3): Show |
6 | HG00280.hp1 HG00741.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+6769T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815295 | |||||||
| chr3:189815361 | A | G | 127 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.297+6835A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815361 | |||||||
| chr3:189815375 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.297+6849C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815375 | |||||||
| chr3:189815403 | A | G | 93 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0083 others(90): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.297+6877A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815403 | |||||||
| chr3:189815420 | T | C | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.297+6894T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815420 | |||||||
| chr3:189815456 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0299 a0001c0001t0001g0356 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+6930T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815456 | |||||||
| chr3:189815474 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+6948G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815474 | |||||||
| chr3:189815508 | T | C | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+6982T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815508 | |||||||
| chr3:189815517 | A | C | 121 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.297+6991A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815517 | |||||||
| chr3:189815556 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.297+7030A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815556 | |||||||
| chr3:189815641 | A | G | 132 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0075 others(129): Show |
132 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+7115A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815641 | |||||||
| chr3:189815645 | G | A | 49 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0108 others(46): Show |
49 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.297+7119G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815645 | |||||||
| chr3:189815687 | G | A | 46 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(43): Show |
46 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.297+7161G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815687 | |||||||
| chr3:189815694 | A | G | 2 | a0001c0001t0004g0090 a0001c0001t0005g0089 |
2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.297+7168A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815694 | |||||||
| chr3:189815696 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+7170G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815696 | |||||||
| chr3:189815804 | A | G | 24 | a0001c0001t0001g0091 a0001c0001t0002g0218 a0001c0001t0002g0225 others(21): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.297+7278A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815804 | |||||||
| chr3:189815848 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.297+7322A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815848 | |||||||
| chr3:189815876 | C | G | 65 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0118 others(62): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.297+7350C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815876 | |||||||
| chr3:189815982 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0362 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.297+7456G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815982 | |||||||
| chr3:189815983 | C | T | 316 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(313): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.297+7457C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189815983 | |||||||
| chr3:189816095 | G | C | 173 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(170): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.297+7569G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816095 | |||||||
| chr3:189816275 | A | C | 162 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+7749A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816275 | |||||||
| chr3:189816309 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+7783C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816309 | |||||||
| chr3:189816310 | G | A | 161 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.297+7784G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816310 | |||||||
| chr3:189816323 | G | T | 1 | a0001c0001t0002g0016 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+7797G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816323 | |||||||
| chr3:189816347 | C | T | 160 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.297+7821C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816347 | |||||||
| chr3:189816382 | A | G | 162 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+7856A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816382 | |||||||
| chr3:189816404 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+7878A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816404 | |||||||
| chr3:189816424 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0005g0161 |
2 | NA18612.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.297+7898G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816424 | |||||||
| chr3:189816448 | C | G | 1 | a0001c0001t0004g0392 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.297+7922C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816448 | |||||||
| chr3:189816493 | C | A | 180 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(177): Show |
181 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.297+7967C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816493 | |||||||
| chr3:189816518 | G | A | 165 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(162): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.297+7992G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816518 | |||||||
| chr3:189816771 | A | G | 3 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 |
3 | HG02523.hp2 NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.297+8245A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816771 | |||||||
| chr3:189816794 | A | G | 247 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(244): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.297+8268A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816794 | |||||||
| chr3:189816832 | T | C | 240 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(237): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.297+8306T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816832 | |||||||
| chr3:189816852 | A | G | 238 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.297+8326A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816852 | |||||||
| chr3:189816854 | C | T | 238 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.297+8328C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816854 | |||||||
| chr3:189816859 | C | A | 238 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.297+8333C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189816859 | |||||||
| chr3:189817001 | T | TG | 226 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(223): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.297+8480dupG | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189817001 | ||||||
| chr3:189817006 | GA | G | 8 | a0001c0001t0001g0153 a0001c0001t0001g0374 a0001c0001t0002g0071 others(5): Show |
8 | HG00544.hp1 HG02970.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+8490delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189817006 | ||||||
| chr3:189817007 | A | G | 14 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0003g0028 others(11): Show |
14 | HG01074.hp1 HG01081.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+8481A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817007 | |||||||
| chr3:189817017 | C | A | 237 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(234): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.297+8491C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817017 | |||||||
| chr3:189817054 | C | A | 39 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(36): Show |
40 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+8528C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817054 | |||||||
| chr3:189817169 | G | C | 1 | a0001c0001t0041g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.297+8643G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817169 | |||||||
| chr3:189817235 | A | G | 237 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(234): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.297+8709A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817235 | |||||||
| chr3:189817253 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.297+8727A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817253 | |||||||
| chr3:189817259 | C | A | 1 | a0001c0001t0017g0160 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.297+8733C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817259 | |||||||
| chr3:189817318 | C | G | 10 | a0001c0001t0001g0356 a0001c0001t0002g0009 a0001c0001t0002g0040 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+8792C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817318 | |||||||
| chr3:189817346 | G | A | 2 | a0001c0001t0002g0242 a0001c0002t0001g0061 |
2 | NA18965.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.297+8820G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817346 | |||||||
| chr3:189817495 | G | A | 165 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(162): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.297+8969G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817495 | |||||||
| chr3:189817577 | G | A | 2 | a0001c0001t0001g0388 a0001c0001t0004g0301 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.297+9051G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817577 | |||||||
| chr3:189817749 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+9223T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817749 | |||||||
| chr3:189817786 | T | A | 2 | a0001c0001t0001g0299 a0001c0001t0003g0358 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+9260T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817786 | |||||||
| chr3:189817845 | A | G | 72 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(69): Show |
72 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.297+9319A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189817845 | |||||||
| chr3:189818017 | A | G | 239 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(236): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.297+9491A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818017 | |||||||
| chr3:189818044 | T | G | 1 | a0001c0001t0048g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.297+9518T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818044 | |||||||
| chr3:189818055 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.297+9529A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818055 | |||||||
| chr3:189818122 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.297+9596A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818122 | |||||||
| chr3:189818122 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0363 a0001c0001t0001g0365 others(2): Show |
5 | NA18943.hp1 NA18975.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+9596A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818122 | |||||||
| chr3:189818247 | T | C | 33 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(30): Show |
33 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.297+9721T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818247 | |||||||
| chr3:189818286 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0276 |
2 | NA18947.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.297+9760A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818286 | |||||||
| chr3:189818289 | A | C | 1 | a0001c0001t0005g0124 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.297+9763A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818289 | |||||||
| chr3:189818340 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+9814A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818340 | |||||||
| chr3:189818419 | G | A | 1 | a0001c0001t0048g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.297+9893G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818419 | |||||||
| chr3:189818472 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.297+9946G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818472 | |||||||
| chr3:189818624 | G | A | 4 | a0001c0001t0002g0256 a0001c0001t0002g0261 a0001c0002t0001g0198 others(1): Show |
4 | NA18939.hp2 NA18945.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+10098G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818624 | |||||||
| chr3:189818624 | G | T | 1 | a0001c0002t0009g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.297+10098G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818624 | |||||||
| chr3:189818684 | A | G | 2 | a0001c0001t0001g0381 a0001c0001t0002g0150 |
2 | NA18974.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.297+10158A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818684 | |||||||
| chr3:189818722 | A | G | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG02970.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.297+10196A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818722 | |||||||
| chr3:189818871 | A | G | 200 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.297+10345A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189818871 | |||||||
| chr3:189819009 | G | A | 1 | a0001c0001t0020g0330 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.297+10483G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819009 | |||||||
| chr3:189819224 | G | C | 1 | a0001c0001t0048g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.297+10698G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819224 | |||||||
| chr3:189819293 | T | A | 39 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(36): Show |
40 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+10767T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819293 | |||||||
| chr3:189819293 | T | TA | 3 | a0001c0001t0002g0294 a0001c0001t0003g0295 a0001c0001t0029g0048 |
3 | HG03098.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+10770dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189819293 | ||||||
| chr3:189819340 | A | G | 15 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0002g0332 others(12): Show |
16 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+10814A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819340 | |||||||
| chr3:189819367 | G | A | 39 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(36): Show |
40 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+10841G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819367 | |||||||
| chr3:189819439 | C | A | 1 | a0001c0001t0026g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.297+10913C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819439 | |||||||
| chr3:189819506 | C | T | 7 | a0001c0001t0001g0298 a0001c0001t0001g0354 a0001c0001t0003g0353 others(4): Show |
7 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+10980C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819506 | |||||||
| chr3:189819510 | G | T | 1 | a0001c0001t0032g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.297+10984G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819510 | |||||||
| chr3:189819590 | A | C | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+11064A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819590 | |||||||
| chr3:189819631 | A | G | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+11105A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819631 | |||||||
| chr3:189819678 | A | G | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+11152A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819678 | |||||||
| chr3:189819732 | T | C | 40 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(37): Show |
41 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.297+11206T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819732 | |||||||
| chr3:189819747 | C | CT | 68 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0087 others(65): Show |
69 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.297+11243dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189819747 | ||||||
| chr3:189819747 | C | CTT | 10 | a0001c0001t0001g0355 a0001c0001t0002g0208 a0001c0001t0002g0209 others(7): Show |
10 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+11242_297+1124 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189819747 | ||||||
| chr3:189819747 | CTTTT | C | 35 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(32): Show |
36 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.297+11240_297+1124 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189819747 | ||||||
| chr3:189819768 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.297+11242T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819768 | |||||||
| chr3:189819768 | T | TC | 187 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.297+11242_297+1124 others(5): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819768 | |||||||
| chr3:189819768 | T | TTC | 11 | a0001c0001t0001g0054 a0001c0001t0001g0371 a0001c0001t0001g0376 others(8): Show |
11 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.297+11243_297+1124 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189819768 | ||||||
| chr3:189819795 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.297+11269A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819795 | |||||||
| chr3:189819820 | G | C | 38 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(35): Show |
39 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.297+11294G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819820 | |||||||
| chr3:189819896 | G | A | 1 | a0001c0001t0019g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.297+11370G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189819896 | |||||||
| chr3:189820001 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+11475G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820001 | |||||||
| chr3:189820079 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+11553A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820079 | |||||||
| chr3:189820099 | C | T | 61 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0153 others(58): Show |
62 | HG00140.hp2 HG00544.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+11573C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820099 | |||||||
| chr3:189820328 | A | G | 17 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0200 others(14): Show |
17 | HG00639.hp2 HG01081.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+11802A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820328 | |||||||
| chr3:189820380 | G | A | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+11854G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820380 | |||||||
| chr3:189820408 | T | G | 37 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(34): Show |
38 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.297+11882T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820408 | |||||||
| chr3:189820451 | C | G | 40 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(37): Show |
41 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.297+11925C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820451 | |||||||
| chr3:189820534 | CTT | C | 18 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.297+12010_297+1201 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189820534 | ||||||
| chr3:189820771 | T | C | 39 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(36): Show |
40 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+12245T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820771 | |||||||
| chr3:189820779 | C | T | 2 | a0001c0001t0004g0109 a0001c0001t0005g0110 |
2 | HG02074.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.297+12253C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820779 | |||||||
| chr3:189820882 | C | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+12356C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189820882 | |||||||
| chr3:189821252 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.297+12726G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189821252 | |||||||
| chr3:189821467 | A | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0012g0296 |
3 | HG02486.hp2 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.297+12941A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189821467 | |||||||
| chr3:189821531 | T | C | 164 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.297+13005T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189821531 | |||||||
| chr3:189821593 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+13067C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189821593 | |||||||
| chr3:189821811 | C | T | 14 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0003g0028 others(11): Show |
14 | HG01074.hp1 HG01081.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+13285C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189821811 | |||||||
| chr3:189822136 | T | C | 164 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.297+13610T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822136 | |||||||
| chr3:189822313 | C | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0302 a0001c0001t0002g0303 |
3 | HG00438.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.297+13787C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822313 | |||||||
| chr3:189822336 | A | T | 1 | a0001c0001t0002g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.297+13810A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822336 | |||||||
| chr3:189822508 | G | A | 162 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+13982G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822508 | |||||||
| chr3:189822567 | T | G | 74 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(71): Show |
74 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.297+14041T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822567 | |||||||
| chr3:189822729 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0136 others(4): Show |
7 | NA18977.hp2 NA19010.hp1 NA19066.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+14203C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822729 | |||||||
| chr3:189822754 | G | A | 1 | a0001c0002t0009g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+14228G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822754 | |||||||
| chr3:189822775 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0003g0011 a0001c0001t0004g0392 |
3 | HG02647.hp1 HG03540.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.297+14249G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189822775 | |||||||
| chr3:189823004 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+14478C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823004 | |||||||
| chr3:189823099 | T | C | 3 | a0001c0001t0002g0294 a0001c0001t0003g0295 a0001c0001t0029g0048 |
3 | HG03098.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+14573T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823099 | |||||||
| chr3:189823403 | G | A | 152 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(149): Show |
153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.297+14877G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823403 | |||||||
| chr3:189823777 | TA | T | 28 | a0001c0001t0001g0099 a0001c0001t0001g0200 a0001c0001t0001g0203 others(25): Show |
28 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.297+15254delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189823777 | ||||||
| chr3:189823839 | A | G | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+15313A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823839 | |||||||
| chr3:189823848 | G | A | 1 | a0001c0001t0044g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.297+15322G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823848 | |||||||
| chr3:189823884 | C | T | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+15358C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823884 | |||||||
| chr3:189823936 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.297+15410T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189823936 | |||||||
| chr3:189824033 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.297+15507C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824033 | |||||||
| chr3:189824080 | C | T | 11 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(8): Show |
11 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+15554C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824080 | |||||||
| chr3:189824137 | T | A | 1 | a0001c0001t0003g0181 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.297+15611T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824137 | |||||||
| chr3:189824196 | T | C | 9 | a0001c0001t0001g0092 a0001c0001t0002g0282 a0001c0001t0007g0283 others(6): Show |
9 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+15670T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824196 | |||||||
| chr3:189824224 | A | T | 3 | a0001c0001t0002g0349 a0001c0001t0012g0038 a0001c0001t0036g0129 |
3 | HG02572.hp1 HG06807.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.297+15698A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824224 | |||||||
| chr3:189824227 | T | A | 165 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(162): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.297+15701T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824227 | |||||||
| chr3:189824230 | T | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0191 |
2 | HG00609.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.297+15704T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824230 | |||||||
| chr3:189824246 | T | G | 1 | a0001c0001t0048g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.297+15720T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824246 | |||||||
| chr3:189824252 | C | T | 163 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+15726C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824252 | |||||||
| chr3:189824320 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.297+15794C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824320 | |||||||
| chr3:189824325 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+15799C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824325 | |||||||
| chr3:189824326 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+15800G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824326 | |||||||
| chr3:189824521 | C | T | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+15995C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824521 | |||||||
| chr3:189824707 | G | A | 1 | a0001c0001t0002g0332 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.297+16181G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824707 | |||||||
| chr3:189824834 | TA | T | 64 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0117 others(61): Show |
65 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.297+16325delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189824834 | ||||||
| chr3:189824925 | G | A | 15 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0002g0332 others(12): Show |
16 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+16399G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824925 | |||||||
| chr3:189824943 | G | A | 1 | a0001c0001t0012g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+16417G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189824943 | |||||||
| chr3:189825026 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.297+16500T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825026 | |||||||
| chr3:189825209 | A | T | 3 | a0001c0001t0002g0294 a0001c0001t0003g0295 a0001c0001t0029g0048 |
3 | HG03098.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+16683A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825209 | |||||||
| chr3:189825299 | A | G | 8 | a0001c0001t0004g0088 a0001c0001t0004g0090 a0001c0001t0005g0089 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+16773A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825299 | |||||||
| chr3:189825347 | T | C | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+16821T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825347 | |||||||
| chr3:189825352 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+16826A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825352 | |||||||
| chr3:189825356 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+16830T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825356 | |||||||
| chr3:189825362 | A | G | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.297+16836A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825362 | |||||||
| chr3:189825364 | A | G | 1 | a0001c0001t0006g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.297+16838A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825364 | |||||||
| chr3:189825487 | T | C | 164 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.297+16961T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825487 | |||||||
| chr3:189825587 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.297+17061C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825587 | |||||||
| chr3:189825796 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.297+17270A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825796 | |||||||
| chr3:189825997 | G | A | 5 | a0001c0001t0002g0218 a0001c0001t0002g0234 a0001c0001t0002g0251 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+17471G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189825997 | |||||||
| chr3:189826185 | C | T | 162 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.297+17659C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826185 | |||||||
| chr3:189826195 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+17669T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826195 | |||||||
| chr3:189826200 | G | A | 1 | a0001c0001t0035g0097 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.297+17674G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826200 | |||||||
| chr3:189826220 | A | G | 175 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.297+17694A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826220 | |||||||
| chr3:189826263 | T | A | 3 | a0001c0001t0001g0354 a0001c0001t0003g0353 a0001c0001t0004g0393 |
3 | HG02717.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.297+17737T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826263 | |||||||
| chr3:189826318 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+17792G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826318 | |||||||
| chr3:189826377 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0362 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.297+17851T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826377 | |||||||
| chr3:189826383 | A | G | 1 | a0001c0001t0003g0351 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+17857A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826383 | |||||||
| chr3:189826426 | T | G | 11 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(8): Show |
11 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+17900T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826426 | |||||||
| chr3:189826471 | C | G | 3 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 |
3 | HG02523.hp2 NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.297+17945C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826471 | |||||||
| chr3:189826476 | A | G | 12 | a0001c0001t0001g0298 a0001c0001t0001g0354 a0001c0001t0002g0071 others(9): Show |
12 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+17950A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826476 | |||||||
| chr3:189826479 | T | G | 163 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+17953T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826479 | |||||||
| chr3:189826500 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.297+17974G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826500 | |||||||
| chr3:189826565 | C | T | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.297+18039C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826565 | |||||||
| chr3:189826612 | A | C | 1 | a0001c0001t0003g0351 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+18086A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826612 | |||||||
| chr3:189826706 | G | A | 28 | a0001c0001t0001g0099 a0001c0001t0001g0200 a0001c0001t0001g0203 others(25): Show |
28 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.297+18180G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826706 | |||||||
| chr3:189826888 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0002g0350 a0001c0001t0003g0351 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+18362C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826888 | |||||||
| chr3:189826987 | A | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+18461A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189826987 | |||||||
| chr3:189827180 | C | G | 6 | a0001c0001t0001g0203 a0001c0001t0002g0350 a0001c0001t0003g0351 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+18654C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827180 | |||||||
| chr3:189827232 | A | G | 11 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(8): Show |
11 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+18706A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827232 | |||||||
| chr3:189827278 | T | G | 344 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.297+18752T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827278 | |||||||
| chr3:189827285 | T | A | 20 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.297+18759T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827285 | |||||||
| chr3:189827462 | A | C | 1 | a0001c0001t0007g0334 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.297+18936A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827462 | |||||||
| chr3:189827546 | T | C | 1 | a0001c0001t0002g0260 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.297+19020T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827546 | |||||||
| chr3:189827593 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.297+19067A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827593 | |||||||
| chr3:189827631 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.297+19105G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827631 | |||||||
| chr3:189827880 | A | G | 2 | a0001c0001t0002g0263 a0001c0001t0003g0133 |
2 | HG02523.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.297+19354A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189827880 | |||||||
| chr3:189828011 | C | G | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.297+19485C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828011 | |||||||
| chr3:189828046 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+19520G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828046 | |||||||
| chr3:189828048 | C | G | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG02970.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.297+19522C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828048 | |||||||
| chr3:189828133 | C | T | 56 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(53): Show |
56 | HG00408.hp2 HG00621.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.297+19607C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828133 | |||||||
| chr3:189828176 | G | C | 2 | a0001c0001t0001g0379 a0001c0001t0039g0232 |
2 | NA18940.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.297+19650G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828176 | |||||||
| chr3:189828206 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+19680G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828206 | |||||||
| chr3:189828228 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.297+19702G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828228 | |||||||
| chr3:189828249 | C | CA | 6 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0002g0044 others(3): Show |
6 | HG02735.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+19737dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189828249 | ||||||
| chr3:189828249 | CA | C | 28 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0180 others(25): Show |
29 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.297+19737delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189828249 | ||||||
| chr3:189828258 | A | C | 3 | a0001c0001t0001g0355 a0001c0001t0003g0013 a0001c0001t0026g0012 |
3 | HG02109.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.297+19732A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828258 | |||||||
| chr3:189828262 | A | AAG | 6 | a0001c0001t0001g0203 a0001c0001t0002g0350 a0001c0001t0003g0351 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+19746_297+1974 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189828262 | ||||||
| chr3:189828271 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+19745A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828271 | |||||||
| chr3:189828428 | T | C | 1 | a0001c0001t0010g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.297+19902T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828428 | |||||||
| chr3:189828600 | C | G | 1 | a0001c0001t0005g0163 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.297+20074C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828600 | |||||||
| chr3:189828830 | G | A | 1 | a0001c0001t0024g0317 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.297+20304G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828830 | |||||||
| chr3:189828879 | A | G | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297+20353A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828879 | |||||||
| chr3:189828987 | C | T | 1 | a0001c0001t0003g0267 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.297+20461C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828987 | |||||||
| chr3:189828990 | G | A | 1 | a0001c0001t0001g0376 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.297+20464G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189828990 | |||||||
| chr3:189829146 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+20620T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829146 | |||||||
| chr3:189829149 | G | T | 2 | a0001c0001t0002g0294 a0001c0001t0003g0295 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+20623G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829149 | |||||||
| chr3:189829180 | G | T | 5 | a0001c0001t0002g0218 a0001c0001t0002g0234 a0001c0001t0002g0251 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+20654G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829180 | |||||||
| chr3:189829323 | C | T | 1 | a0001c0001t0003g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.297+20797C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829323 | |||||||
| chr3:189829369 | T | G | 2 | a0001c0001t0001g0326 a0001c0001t0001g0328 |
2 | NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.297+20843T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829369 | |||||||
| chr3:189829401 | A | T | 1 | a0001c0001t0002g0238 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.297+20875A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829401 | |||||||
| chr3:189829404 | C | G | 163 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+20878C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829404 | |||||||
| chr3:189829437 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.297+20911A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829437 | |||||||
| chr3:189829450 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0004g0149 |
3 | HG00280.hp1 HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.297+20924A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829450 | |||||||
| chr3:189829798 | T | C | 163 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+21272T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829798 | |||||||
| chr3:189829863 | A | G | 160 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.297+21337A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829863 | |||||||
| chr3:189829908 | A | G | 16 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0002g0225 others(13): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.297+21382A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829908 | |||||||
| chr3:189829946 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+21420T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829946 | |||||||
| chr3:189829989 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0003g0247 a0001c0001t0003g0248 others(3): Show |
6 | NA18747.hp2 NA18940.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+21463C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189829989 | |||||||
| chr3:189830084 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0003g0068 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.297+21558G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830084 | |||||||
| chr3:189830120 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+21594A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830120 | |||||||
| chr3:189830135 | A | G | 1 | a0001c0001t0007g0286 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.297+21609A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830135 | |||||||
| chr3:189830171 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0363 a0001c0001t0001g0365 others(2): Show |
5 | NA18943.hp1 NA18975.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+21645T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830171 | |||||||
| chr3:189830242 | G | A | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+21716G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830242 | |||||||
| chr3:189830331 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0164 |
2 | HG03098.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.297+21805A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830331 | |||||||
| chr3:189830641 | GC | G | 9 | a0001c0001t0001g0298 a0001c0001t0001g0354 a0001c0001t0002g0071 others(6): Show |
9 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+22117delC | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189830641 | ||||||
| chr3:189830672 | A | G | 74 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(71): Show |
74 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.297+22146A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830672 | |||||||
| chr3:189830739 | A | G | 1 | a0001c0001t0003g0002 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.297+22213A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830739 | |||||||
| chr3:189830758 | A | G | 187 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(184): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.297+22232A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830758 | |||||||
| chr3:189830972 | T | C | 16 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0002g0225 others(13): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.297+22446T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189830972 | |||||||
| chr3:189831003 | A | G | 166 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(163): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.297+22477A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831003 | |||||||
| chr3:189831062 | CTGT | C | 13 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(10): Show |
13 | HG00621.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.297+22542_297+2254 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831062 | ||||||
| chr3:189831073 | G | A | 15 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0002g0332 others(12): Show |
16 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+22547G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831073 | |||||||
| chr3:189831095 | A | T | 9 | a0001c0001t0001g0141 a0001c0001t0001g0357 a0001c0001t0001g0384 others(6): Show |
9 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+22569A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831095 | |||||||
| chr3:189831246 | G | A | 1 | a0001c0001t0047g0235 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+22720G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831246 | |||||||
| chr3:189831293 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+22767C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831293 | |||||||
| chr3:189831461 | T | C | 1 | a0001c0001t0012g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.297+22935T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831461 | |||||||
| chr3:189831560 | C | T | 9 | a0001c0001t0001g0298 a0001c0001t0001g0354 a0001c0001t0002g0071 others(6): Show |
9 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+23034C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831560 | |||||||
| chr3:189831634 | A | G | 21 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0298 others(18): Show |
21 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+23108A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831634 | |||||||
| chr3:189831761 | G | A | 1 | a0001c0001t0005g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.297+23235G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831761 | |||||||
| chr3:189831818 | C | CT | 39 | a0001c0001t0001g0055 a0001c0001t0001g0135 a0001c0001t0001g0159 others(36): Show |
39 | HG00735.hp2 HG00738.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.297+23321dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CT | C | 49 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0080 others(46): Show |
49 | HG00639.hp2 HG01069.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.297+23321delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CTT | C | 73 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0091 others(70): Show |
75 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.297+23320_297+2332 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CTTTT | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(4): Show |
7 | HG00544.hp1 HG02523.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+23318_297+2332 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CTTTTT | C | 6 | a0001c0001t0001g0354 a0001c0001t0002g0042 a0001c0001t0003g0353 others(3): Show |
6 | HG01256.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+23317_297+2332 others(9): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CTTTTTT | C | 6 | a0001c0001t0001g0298 a0001c0001t0002g0071 a0001c0001t0002g0072 others(3): Show |
6 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+23316_297+2332 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831818 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0003g0013 a0001c0001t0026g0012 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.297+23303_297+2332 others(23): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189831818 | ||||||
| chr3:189831820 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.297+23294T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831820 | |||||||
| chr3:189831901 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.297+23375G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189831901 | |||||||
| chr3:189832116 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+23590C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832116 | |||||||
| chr3:189832161 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+23635T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832161 | |||||||
| chr3:189832253 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+23727C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832253 | |||||||
| chr3:189832386 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+23860G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832386 | |||||||
| chr3:189832387 | T | C | 22 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0312 others(19): Show |
22 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.297+23861T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832387 | |||||||
| chr3:189832412 | C | G | 22 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0312 others(19): Show |
22 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.297+23886C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832412 | |||||||
| chr3:189832579 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.297+24053G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832579 | |||||||
| chr3:189832683 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+24157T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832683 | |||||||
| chr3:189832697 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.297+24171G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832697 | |||||||
| chr3:189832862 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.297+24336A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832862 | |||||||
| chr3:189832905 | A | T | 1 | a0001c0001t0002g0350 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+24379A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832905 | |||||||
| chr3:189832981 | A | T | 1 | a0001c0001t0003g0254 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+24455A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189832981 | |||||||
| chr3:189833012 | A | C | 24 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0312 others(21): Show |
24 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+24486A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833012 | |||||||
| chr3:189833159 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+24633T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833159 | |||||||
| chr3:189833163 | T | C | 11 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(8): Show |
11 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+24637T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833163 | |||||||
| chr3:189833228 | G | A | 1 | a0001c0001t0020g0284 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.297+24702G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833228 | |||||||
| chr3:189833460 | A | G | 4 | a0001c0001t0001g0298 a0001c0001t0002g0294 a0001c0001t0003g0295 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+24934A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833460 | |||||||
| chr3:189833551 | C | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+25025C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833551 | |||||||
| chr3:189833631 | A | G | 50 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0091 others(47): Show |
51 | HG00140.hp2 HG00544.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.297+25105A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833631 | |||||||
| chr3:189833678 | CT | C | 226 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(223): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.297+25166delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189833678 | ||||||
| chr3:189833678 | CTT | C | 62 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0091 others(59): Show |
63 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.297+25165_297+2516 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189833678 | ||||||
| chr3:189833692 | T | A | 5 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(2): Show |
5 | HG02970.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+25166T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833692 | |||||||
| chr3:189833750 | T | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0203 a0001c0001t0004g0074 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+25224T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189833750 | |||||||
| chr3:189834078 | C | T | 1 | a0001c0001t0004g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.297+25552C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834078 | |||||||
| chr3:189834079 | G | A | 1 | a0001c0001t0006g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.297+25553G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834079 | |||||||
| chr3:189834293 | C | A | 1 | a0001c0001t0010g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.297+25767C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834293 | |||||||
| chr3:189834372 | A | G | 181 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(178): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.297+25846A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834372 | |||||||
| chr3:189834447 | T | C | 203 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(200): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.297+25921T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834447 | |||||||
| chr3:189834484 | C | A | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25958C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834484 | |||||||
| chr3:189834485 | C | T | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25959C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834485 | |||||||
| chr3:189834486 | T | A | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25960T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834486 | |||||||
| chr3:189834488 | C | A | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25962C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834488 | |||||||
| chr3:189834491 | A | G | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25965A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834491 | |||||||
| chr3:189834493 | A | G | 1 | a0001c0001t0001g0379 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297+25967A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834493 | |||||||
| chr3:189834530 | C | T | 1 | a0001c0001t0042g0333 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.297+26004C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834530 | |||||||
| chr3:189834582 | A | G | 177 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.297+26056A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834582 | |||||||
| chr3:189834608 | C | T | 1 | a0001c0001t0005g0377 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.297+26082C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834608 | |||||||
| chr3:189834689 | C | G | 12 | a0001c0001t0001g0092 a0001c0001t0001g0312 a0001c0001t0002g0282 others(9): Show |
12 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+26163C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834689 | |||||||
| chr3:189834731 | CAG | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(6): Show |
9 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+26208_297+2620 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189834731 | ||||||
| chr3:189834781 | C | T | 177 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.297+26255C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834781 | |||||||
| chr3:189834834 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.297+26308T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834834 | |||||||
| chr3:189834863 | A | G | 177 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.297+26337A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834863 | |||||||
| chr3:189834888 | C | CT | 10 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0199 others(7): Show |
10 | HG00544.hp1 HG00639.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+26375dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189834888 | ||||||
| chr3:189834888 | C | CTT | 12 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0003g0028 others(9): Show |
12 | HG01074.hp1 HG01081.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+26374_297+2637 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189834888 | ||||||
| chr3:189834888 | C | CTTT | 154 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(151): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.297+26373_297+2637 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189834888 | ||||||
| chr3:189834938 | G | A | 1 | a0001c0001t0008g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.297+26412G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189834938 | |||||||
| chr3:189835067 | C | T | 2 | a0001c0001t0002g0343 a0001c0001t0007g0342 |
2 | HG00140.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.297+26541C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835067 | |||||||
| chr3:189835108 | A | G | 5 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(2): Show |
5 | HG02970.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+26582A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835108 | |||||||
| chr3:189835159 | C | T | 351 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(348): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.297+26633C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835159 | |||||||
| chr3:189835266 | ACTC | A | 14 | a0001c0001t0001g0298 a0001c0001t0001g0385 a0001c0001t0002g0071 others(11): Show |
14 | HG02280.hp1 HG02615.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+26743_297+2674 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835266 | ||||||
| chr3:189835337 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.297+26811G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835337 | |||||||
| chr3:189835498 | C | T | 47 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0117 others(44): Show |
48 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.297+26972C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835498 | |||||||
| chr3:189835506 | T | C | 7 | a0001c0001t0001g0384 a0001c0001t0001g0394 a0001c0001t0010g0352 others(4): Show |
7 | HG02451.hp2 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+26980T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835506 | |||||||
| chr3:189835544 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.297+27018G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835544 | |||||||
| chr3:189835547 | G | T | 349 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.297+27021G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835547 | |||||||
| chr3:189835583 | C | T | 8 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(5): Show |
8 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+27057C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835583 | |||||||
| chr3:189835728 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+27202C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835728 | |||||||
| chr3:189835804 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.297+27278C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835804 | |||||||
| chr3:189835915 | AAAT | A | 111 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.297+27441_297+2744 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAAT | A | 47 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(44): Show |
47 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.297+27438_297+2744 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAATA others(2): Show |
A | 44 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.297+27435_297+2744 others(13): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAATA others(5): Show |
A | 30 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0138 others(27): Show |
31 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.297+27432_297+2744 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAATA others(8): Show |
A | 41 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0117 others(38): Show |
42 | HG00099.hp2 HG00738.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.297+27429_297+2744 others(19): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAATA others(11): Show |
A | 1 | a0001c0001t0001g0354 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+27426_297+2744 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835915 | AAATAATA others(17): Show |
A | 5 | a0001c0001t0001g0298 a0001c0001t0002g0294 a0001c0001t0003g0295 others(2): Show |
5 | HG02615.hp2 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+27420_297+2744 others(28): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835915 | ||||||
| chr3:189835958 | A | G | 1 | a0001c0001t0042g0333 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.297+27432A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835958 | |||||||
| chr3:189835964 | A | AATAATAA others(5): Show |
1 | a0001c0001t0002g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.297+27443_297+2744 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835964 | ||||||
| chr3:189835964 | A | AATAATG | 8 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0002g0276 others(5): Show |
8 | HG02015.hp2 HG03225.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+27439_297+2744 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835964 | ||||||
| chr3:189835964 | A | AATG | 32 | a0001c0001t0001g0043 a0001c0001t0001g0355 a0001c0001t0001g0389 others(29): Show |
32 | HG00423.hp2 HG00741.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.297+27440_297+2744 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189835964 | ||||||
| chr3:189835964 | A | G | 246 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(243): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.297+27438A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189835964 | |||||||
| chr3:189836001 | C | A | 182 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(179): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.297+27475C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836001 | |||||||
| chr3:189836026 | A | G | 8 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0374 others(5): Show |
8 | HG00544.hp1 HG01256.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+27500A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836026 | |||||||
| chr3:189836070 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.297+27544G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836070 | |||||||
| chr3:189836311 | G | T | 8 | a0001c0001t0001g0356 a0001c0001t0002g0009 a0001c0001t0002g0069 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+27785G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836311 | |||||||
| chr3:189836330 | A | C | 5 | a0001c0001t0001g0298 a0001c0001t0002g0294 a0001c0001t0003g0295 others(2): Show |
5 | HG02615.hp2 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+27804A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836330 | |||||||
| chr3:189836427 | A | T | 1 | a0001c0001t0004g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.298-27805A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836427 | |||||||
| chr3:189836813 | G | A | 3 | a0001c0001t0011g0076 a0001c0001t0034g0280 a0001c0001t0040g0348 |
3 | HG03453.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.298-27419G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836813 | |||||||
| chr3:189836851 | C | T | 1 | a0001c0001t0004g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.298-27381C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836851 | |||||||
| chr3:189836857 | G | A | 173 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(170): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.298-27375G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836857 | |||||||
| chr3:189836968 | T | G | 168 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.298-27264T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189836968 | |||||||
| chr3:189837084 | G | C | 47 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0117 others(44): Show |
48 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.298-27148G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837084 | |||||||
| chr3:189837088 | C | T | 8 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(5): Show |
8 | HG02559.hp1 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-27144C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837088 | |||||||
| chr3:189837105 | T | C | 115 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(112): Show |
115 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.298-27127T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837105 | |||||||
| chr3:189837132 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.298-27100C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837132 | |||||||
| chr3:189837208 | A | AT | 73 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(70): Show |
73 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.298-27014dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189837208 | ||||||
| chr3:189837424 | C | T | 1 | a0001c0001t0025g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.298-26808C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837424 | |||||||
| chr3:189837451 | C | CAAATTAA others(21): Show |
175 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.298-26766_298-2673 others(32): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189837451 | ||||||
| chr3:189837731 | G | A | 1 | a0001c0001t0028g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.298-26501G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837731 | |||||||
| chr3:189837845 | G | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(3): Show |
6 | HG01175.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-26387G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837845 | |||||||
| chr3:189837861 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-26371G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837861 | |||||||
| chr3:189837972 | T | A | 1 | a0001c0001t0001g0371 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.298-26260T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189837972 | |||||||
| chr3:189838140 | G | T | 49 | a0001c0001t0001g0043 a0001c0001t0001g0141 a0001c0001t0001g0200 others(46): Show |
49 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.298-26092G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838140 | |||||||
| chr3:189838172 | T | C | 172 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(169): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.298-26060T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838172 | |||||||
| chr3:189838205 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.298-26027T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838205 | |||||||
| chr3:189838392 | T | C | 1 | a0001c0001t0002g0332 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.298-25840T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838392 | |||||||
| chr3:189838405 | C | T | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298-25827C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838405 | |||||||
| chr3:189838445 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.298-25787C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838445 | |||||||
| chr3:189838636 | G | A | 11 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0231 others(8): Show |
11 | HG01074.hp1 HG01081.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-25596G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838636 | |||||||
| chr3:189838882 | C | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-25350C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838882 | |||||||
| chr3:189838907 | A | G | 68 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(65): Show |
68 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.298-25325A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838907 | |||||||
| chr3:189838913 | A | G | 6 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(3): Show |
6 | HG02970.hp2 HG03139.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-25319A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838913 | |||||||
| chr3:189838921 | A | G | 40 | a0001c0001t0001g0087 a0001c0001t0001g0117 a0001c0001t0001g0154 others(37): Show |
41 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.298-25311A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189838921 | |||||||
| chr3:189839017 | A | G | 179 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(176): Show |
180 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.298-25215A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839017 | |||||||
| chr3:189839040 | T | TA | 9 | a0001c0001t0001g0081 a0001c0001t0001g0298 a0001c0001t0001g0328 others(6): Show |
9 | HG01261.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-25168dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189839040 | ||||||
| chr3:189839040 | TA | T | 167 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(164): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.298-25168delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189839040 | ||||||
| chr3:189839040 | TAA | T | 10 | a0001c0001t0001g0114 a0001c0001t0001g0138 a0001c0001t0001g0193 others(7): Show |
10 | HG00140.hp2 HG01069.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-25169_298-2516 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189839040 | ||||||
| chr3:189839057 | A | G | 1 | a0001c0001t0034g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-25175A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839057 | |||||||
| chr3:189839059 | A | AG | 59 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.298-25173_298-2517 others(5): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839059 | |||||||
| chr3:189839059 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0002g0233 a0001c0001t0008g0306 others(2): Show |
5 | HG01943.hp1 HG01943.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-25173A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839059 | |||||||
| chr3:189839079 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0385 a0001c0001t0010g0387 |
3 | HG02280.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.298-25153A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839079 | |||||||
| chr3:189839092 | C | A | 6 | a0001c0001t0003g0035 a0001c0001t0003g0037 a0001c0001t0003g0347 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-25140C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839092 | |||||||
| chr3:189839451 | G | A | 12 | a0001c0001t0001g0063 a0001c0001t0001g0179 a0001c0001t0001g0376 others(9): Show |
12 | HG00597.hp1 HG02074.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-24781G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839451 | |||||||
| chr3:189839743 | C | T | 1 | a0001c0001t0020g0284 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.298-24489C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839743 | |||||||
| chr3:189839777 | A | G | 3 | a0001c0001t0001g0357 a0001c0001t0010g0098 a0001c0001t0013g0201 |
3 | HG01884.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.298-24455A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839777 | |||||||
| chr3:189839861 | C | T | 11 | a0001c0001t0001g0087 a0001c0001t0001g0114 a0001c0001t0001g0122 others(8): Show |
11 | HG01256.hp2 HG01993.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-24371C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839861 | |||||||
| chr3:189839897 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0369 |
2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.298-24335G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839897 | |||||||
| chr3:189839898 | C | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0369 |
2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.298-24334C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189839898 | |||||||
| chr3:189840186 | G | A | 1 | a0001c0001t0048g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.298-24046G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840186 | |||||||
| chr3:189840297 | T | C | 4 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 others(1): Show |
4 | NA18940.hp2 NA18952.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-23935T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840297 | |||||||
| chr3:189840320 | G | C | 46 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(43): Show |
46 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.298-23912G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840320 | |||||||
| chr3:189840354 | TTCG | T | 49 | a0001c0001t0001g0043 a0001c0001t0001g0118 a0001c0001t0001g0173 others(46): Show |
49 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.298-23875_298-2387 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840354 | ||||||
| chr3:189840356 | CGTCT | C | 3 | a0001c0001t0001g0050 a0001c0001t0002g0268 a0001c0001t0014g0079 |
3 | HG01070.hp2 HG01496.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.298-23875_298-2387 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840356 | |||||||
| chr3:189840356 | CGTCTTTT | C | 46 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(43): Show |
46 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.298-23875_298-2386 others(11): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840356 | |||||||
| chr3:189840356 | CGTCTTTT others(3): Show |
C | 1 | a0001c0001t0002g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.298-23875_298-2386 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840356 | |||||||
| chr3:189840357 | G | T | 120 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(117): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.298-23875G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840357 | |||||||
| chr3:189840359 | C | CT | 71 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0087 others(68): Show |
72 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.298-23845dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840359 | ||||||
| chr3:189840359 | C | CTT | 14 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0001g0138 others(11): Show |
14 | HG00408.hp2 HG01884.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.298-23846_298-2384 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840359 | ||||||
| chr3:189840359 | CT | C | 126 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0053 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.298-23845delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840359 | ||||||
| chr3:189840359 | CTT | C | 32 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0083 others(29): Show |
32 | HG00438.hp2 HG00733.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-23846_298-2384 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840359 | ||||||
| chr3:189840359 | CTTT | C | 12 | a0001c0001t0001g0122 a0001c0001t0001g0320 a0001c0001t0001g0374 others(9): Show |
12 | HG00544.hp1 HG01993.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-23847_298-2384 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840359 | ||||||
| chr3:189840362 | T | C | 49 | a0001c0001t0001g0043 a0001c0001t0001g0118 a0001c0001t0001g0173 others(46): Show |
49 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.298-23870T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840362 | |||||||
| chr3:189840363 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0002g0268 a0001c0001t0014g0079 |
3 | HG01070.hp2 HG01496.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.298-23869T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840363 | |||||||
| chr3:189840366 | T | C | 46 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(43): Show |
46 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.298-23866T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840366 | |||||||
| chr3:189840368 | T | C | 2 | a0001c0001t0001g0356 a0001c0001t0011g0076 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.298-23864T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840368 | |||||||
| chr3:189840369 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.298-23863T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840369 | |||||||
| chr3:189840492 | CAGAG | C | 72 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0125 others(69): Show |
72 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.298-23732_298-2372 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840492 | ||||||
| chr3:189840626 | T | C | 1 | a0001c0001t0003g0358 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.298-23606T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840626 | |||||||
| chr3:189840642 | C | T | 20 | a0001c0001t0001g0135 a0001c0001t0002g0234 a0001c0001t0002g0332 others(17): Show |
20 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-23590C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840642 | |||||||
| chr3:189840689 | G | C | 160 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(157): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.298-23543G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840689 | |||||||
| chr3:189840715 | G | A | 1 | a0001c0001t0011g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298-23517G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840715 | |||||||
| chr3:189840789 | A | G | 199 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.298-23443A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840789 | |||||||
| chr3:189840857 | C | CA | 33 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0064 others(30): Show |
33 | HG00423.hp2 HG00738.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.298-23354dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840857 | ||||||
| chr3:189840857 | CAAA | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0183 a0001c0001t0002g0172 others(8): Show |
11 | HG01175.hp2 HG01257.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-23356_298-2335 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840857 | ||||||
| chr3:189840857 | CAAAA | C | 184 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(181): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.298-23357_298-2335 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189840857 | ||||||
| chr3:189840878 | A | C | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.298-23354A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840878 | |||||||
| chr3:189840902 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.298-23330A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840902 | |||||||
| chr3:189840912 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.298-23320G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189840912 | |||||||
| chr3:189841153 | T | C | 1 | a0001c0001t0008g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.298-23079T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841153 | |||||||
| chr3:189841307 | T | C | 14 | a0001c0001t0001g0122 a0001c0001t0001g0320 a0001c0001t0001g0374 others(11): Show |
14 | HG00544.hp1 HG01256.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.298-22925T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841307 | |||||||
| chr3:189841497 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.298-22735A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841497 | |||||||
| chr3:189841547 | G | C | 3 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0022g0325 |
3 | HG00639.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.298-22685G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841547 | |||||||
| chr3:189841547 | G | T | 1 | a0001c0001t0002g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-22685G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841547 | |||||||
| chr3:189841647 | T | C | 3 | a0001c0001t0003g0027 a0001c0001t0026g0022 a0001c0001t0038g0033 |
3 | HG02145.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.298-22585T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841647 | |||||||
| chr3:189841893 | G | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0328 a0001c0001t0001g0329 |
3 | NA19000.hp1 NA19077.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.298-22339G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841893 | |||||||
| chr3:189841953 | C | T | 23 | a0001c0001t0001g0054 a0001c0001t0001g0075 a0001c0001t0001g0081 others(20): Show |
23 | HG00639.hp2 HG01099.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.298-22279C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841953 | |||||||
| chr3:189841968 | G | A | 236 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.298-22264G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189841968 | |||||||
| chr3:189842060 | C | G | 17 | a0001c0001t0002g0225 a0001c0001t0002g0234 a0001c0001t0002g0332 others(14): Show |
17 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.298-22172C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842060 | |||||||
| chr3:189842061 | G | A | 1 | a0001c0001t0003g0395 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298-22171G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842061 | |||||||
| chr3:189842064 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0162 |
2 | NA18959.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.298-22168G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842064 | |||||||
| chr3:189842402 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.298-21830C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842402 | |||||||
| chr3:189842434 | C | T | 2 | a0001c0001t0003g0011 a0001c0001t0010g0352 |
2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.298-21798C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842434 | |||||||
| chr3:189842551 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-21681G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842551 | |||||||
| chr3:189842750 | T | C | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.298-21482T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842750 | |||||||
| chr3:189842800 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.298-21432A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842800 | |||||||
| chr3:189842828 | A | G | 155 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0055 others(152): Show |
156 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.298-21404A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189842828 | |||||||
| chr3:189843246 | C | T | 40 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0113 others(37): Show |
41 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.298-20986C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843246 | |||||||
| chr3:189843259 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-20973G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843259 | |||||||
| chr3:189843289 | G | GGGCT | 47 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0152 others(44): Show |
47 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.298-20942_298-2093 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189843289 | ||||||
| chr3:189843360 | G | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0153 a0001c0001t0001g0206 others(4): Show |
7 | HG03130.hp1 HG03225.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-20872G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843360 | |||||||
| chr3:189843439 | G | A | 6 | a0001c0001t0002g0218 a0001c0001t0002g0251 a0001c0001t0007g0340 others(3): Show |
6 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-20793G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843439 | |||||||
| chr3:189843534 | A | G | 49 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(46): Show |
49 | HG00609.hp1 HG01081.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.298-20698A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843534 | |||||||
| chr3:189843582 | A | G | 1 | a0001c0001t0020g0288 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.298-20650A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843582 | |||||||
| chr3:189843584 | G | A | 2 | a0001c0001t0001g0376 a0001c0001t0002g0256 |
2 | NA18612.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.298-20648G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843584 | |||||||
| chr3:189843610 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0002g0127 |
2 | HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.298-20622C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843610 | |||||||
| chr3:189843725 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298-20507G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843725 | |||||||
| chr3:189843910 | G | T | 1 | a0001c0001t0021g0337 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298-20322G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843910 | |||||||
| chr3:189843989 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.298-20243C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189843989 | |||||||
| chr3:189844173 | CT | C | 71 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0055 others(68): Show |
72 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.298-20047delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189844173 | ||||||
| chr3:189844233 | A | G | 9 | a0001c0001t0001g0043 a0001c0001t0001g0355 a0001c0001t0002g0009 others(6): Show |
9 | HG02280.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-19999A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844233 | |||||||
| chr3:189844318 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298-19914C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844318 | |||||||
| chr3:189844406 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298-19826C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844406 | |||||||
| chr3:189844529 | G | A | 3 | a0001c0001t0003g0210 a0001c0001t0003g0254 a0001c0001t0004g0109 |
3 | HG00423.hp2 HG02074.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.298-19703G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844529 | |||||||
| chr3:189844530 | A | C | 192 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0080 others(189): Show |
193 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.298-19702A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844530 | |||||||
| chr3:189844533 | C | T | 1 | a0001c0005t0002g0246 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.298-19699C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844533 | |||||||
| chr3:189844599 | A | T | 1 | a0001c0001t0025g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.298-19633A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844599 | |||||||
| chr3:189844608 | A | T | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.298-19624A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844608 | |||||||
| chr3:189844721 | A | T | 1 | a0001c0001t0003g0002 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.298-19511A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844721 | |||||||
| chr3:189844881 | T | C | 204 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(201): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.298-19351T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189844881 | |||||||
| chr3:189845215 | A | G | 1 | a0001c0001t0005g0158 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.298-19017A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845215 | |||||||
| chr3:189845228 | A | G | 1 | a0001c0001t0022g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298-19004A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845228 | |||||||
| chr3:189845294 | A | G | 1 | a0001c0001t0011g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298-18938A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845294 | |||||||
| chr3:189845337 | C | T | 4 | a0001c0001t0003g0027 a0001c0001t0010g0387 a0001c0001t0026g0022 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-18895C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845337 | |||||||
| chr3:189845341 | G | A | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298-18891G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845341 | |||||||
| chr3:189845415 | T | C | 129 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0087 others(126): Show |
130 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.298-18817T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845415 | |||||||
| chr3:189845606 | G | A | 1 | a0001c0001t0044g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-18626G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845606 | |||||||
| chr3:189845645 | T | A | 1 | a0001c0001t0002g0268 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.298-18587T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845645 | |||||||
| chr3:189845741 | A | G | 209 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(206): Show |
210 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.298-18491A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845741 | |||||||
| chr3:189845892 | A | T | 208 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(205): Show |
209 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.298-18340A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845892 | |||||||
| chr3:189845986 | C | T | 1 | a0001c0001t0011g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298-18246C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189845986 | |||||||
| chr3:189846003 | A | C | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.298-18229A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846003 | |||||||
| chr3:189846190 | C | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0363 a0001c0001t0001g0365 others(1): Show |
4 | NA18975.hp1 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-18042C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846190 | |||||||
| chr3:189846511 | T | A | 85 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0001g0108 others(82): Show |
86 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.298-17721T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846511 | |||||||
| chr3:189846611 | G | GGT | 88 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0062 others(85): Show |
89 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.298-17588_298-1758 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846611 | G | GGTGT | 10 | a0001c0001t0001g0184 a0001c0001t0001g0194 a0001c0001t0001g0328 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-17590_298-1758 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846611 | GGTGT | G | 63 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0117 others(60): Show |
63 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.298-17590_298-1758 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846611 | GGTGTGT | G | 69 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0099 others(66): Show |
69 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.298-17592_298-1758 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846611 | GGTGTGTG others(7): Show |
G | 4 | a0001c0001t0001g0056 a0001c0001t0002g0336 a0001c0001t0002g0343 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-17600_298-1758 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846611 | GGTGTGTG others(9): Show |
G | 72 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0119 others(69): Show |
73 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.298-17602_298-1758 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846611 | ||||||
| chr3:189846617 | T | G | 1 | a0001c0002t0009g0364 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.298-17615T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846617 | |||||||
| chr3:189846619 | T | G | 3 | a0001c0001t0001g0356 a0001c0001t0018g0070 a0001c0001t0029g0048 |
3 | HG01109.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.298-17613T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846619 | |||||||
| chr3:189846638 | G | C | 47 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(44): Show |
47 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.298-17594G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846638 | |||||||
| chr3:189846682 | C | CT | 90 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0091 others(87): Show |
90 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.298-17526dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846682 | ||||||
| chr3:189846682 | C | CTT | 6 | a0001c0001t0001g0357 a0001c0001t0002g0175 a0001c0001t0010g0387 others(3): Show |
6 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-17527_298-1752 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846682 | ||||||
| chr3:189846682 | CT | C | 90 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0087 others(87): Show |
91 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.298-17526delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846682 | ||||||
| chr3:189846682 | CTT | C | 101 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(98): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.298-17527_298-1752 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846682 | ||||||
| chr3:189846682 | CTTT | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0322 a0001c0001t0002g0272 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-17528_298-1752 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189846682 | ||||||
| chr3:189846718 | A | G | 3 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0034g0280 |
3 | HG02257.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-17514A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846718 | |||||||
| chr3:189846788 | G | A | 1 | a0001c0003t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-17444G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846788 | |||||||
| chr3:189846791 | A | G | 41 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0117 others(38): Show |
41 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.298-17441A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846791 | |||||||
| chr3:189846916 | T | C | 323 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.298-17316T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846916 | |||||||
| chr3:189846917 | G | A | 84 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0001g0108 others(81): Show |
85 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.298-17315G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846917 | |||||||
| chr3:189846985 | A | G | 85 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0001g0108 others(82): Show |
86 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.298-17247A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189846985 | |||||||
| chr3:189847014 | G | A | 3 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0034g0280 |
3 | HG02257.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-17218G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847014 | |||||||
| chr3:189847175 | T | C | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-17057T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847175 | |||||||
| chr3:189847289 | C | T | 13 | a0001c0001t0002g0225 a0001c0001t0003g0181 a0001c0001t0007g0006 others(10): Show |
13 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-16943C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847289 | |||||||
| chr3:189847290 | A | G | 117 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(114): Show |
117 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.298-16942A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847290 | |||||||
| chr3:189847352 | A | C | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-16880A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847352 | |||||||
| chr3:189847375 | C | A | 104 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(101): Show |
104 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.298-16857C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847375 | |||||||
| chr3:189847378 | C | A | 91 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0064 others(88): Show |
91 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.298-16854C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847378 | |||||||
| chr3:189847532 | A | G | 12 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0002g0009 others(9): Show |
12 | HG00639.hp2 HG02280.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-16700A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847532 | |||||||
| chr3:189847577 | C | A | 1 | a0001c0001t0004g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.298-16655C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847577 | |||||||
| chr3:189847589 | T | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG00733.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-16643T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847589 | |||||||
| chr3:189847655 | A | C | 16 | a0001c0001t0002g0222 a0001c0001t0003g0047 a0001c0001t0003g0264 others(13): Show |
16 | HG01175.hp1 HG01433.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-16577A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847655 | |||||||
| chr3:189847663 | A | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0153 others(60): Show |
64 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.298-16569A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847663 | |||||||
| chr3:189847693 | T | C | 33 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0384 others(30): Show |
33 | HG00639.hp2 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.298-16539T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847693 | |||||||
| chr3:189847735 | A | G | 51 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(48): Show |
51 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.298-16497A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847735 | |||||||
| chr3:189847758 | T | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0124 |
2 | HG02083.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.298-16474T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847758 | |||||||
| chr3:189847900 | G | A | 318 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(315): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.298-16332G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189847900 | |||||||
| chr3:189848051 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.298-16181A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848051 | |||||||
| chr3:189848237 | C | T | 4 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-15995C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848237 | |||||||
| chr3:189848239 | T | TCTC | 4 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-15993_298-1599 others(7): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848239 | |||||||
| chr3:189848239 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0002g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.298-15993_298-1599 others(23): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848239 | |||||||
| chr3:189848239 | T | TCTCTCTC others(14): Show |
2 | a0001c0001t0001g0058 a0001c0001t0002g0375 |
2 | HG01168.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.298-15993_298-1599 others(25): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848239 | |||||||
| chr3:189848239 | T | TCTCTCTC others(22): Show |
1 | a0001c0001t0004g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.298-15993_298-1599 others(33): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848239 | |||||||
| chr3:189848239 | T | TTC | 8 | a0001c0001t0001g0140 a0001c0001t0002g0034 a0001c0001t0002g0042 others(5): Show |
8 | HG00140.hp2 HG01099.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-15963_298-1596 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTC | 25 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0156 others(22): Show |
25 | HG00609.hp1 HG02074.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.298-15967_298-1596 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(3): Show |
23 | a0001c0001t0001g0155 a0001c0001t0001g0173 a0001c0001t0002g0242 others(20): Show |
23 | HG01243.hp2 HG01261.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.298-15971_298-1596 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(5): Show |
9 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0002g0040 others(6): Show |
9 | HG00639.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-15973_298-1596 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(7): Show |
25 | a0001c0001t0001g0063 a0001c0001t0001g0080 a0001c0001t0001g0091 others(22): Show |
25 | HG00544.hp2 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-15975_298-1596 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(9): Show |
18 | a0001c0001t0001g0128 a0001c0001t0002g0229 a0001c0001t0002g0234 others(15): Show |
18 | HG00408.hp1 HG00741.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.298-15977_298-1596 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(11): Show |
30 | a0001c0001t0001g0050 a0001c0001t0001g0113 a0001c0001t0001g0125 others(27): Show |
31 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.298-15979_298-1596 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(13): Show |
39 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0083 others(36): Show |
40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.298-15981_298-1596 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(15): Show |
15 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0184 others(12): Show |
15 | HG00544.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.298-15983_298-1596 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(17): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0134 a0001c0001t0008g0323 others(2): Show |
5 | HG01099.hp1 NA18945.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-15985_298-1596 others(28): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(19): Show |
7 | a0001c0001t0001g0141 a0001c0001t0001g0299 a0001c0001t0001g0354 others(4): Show |
7 | HG00673.hp1 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-15987_298-1596 others(30): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(21): Show |
8 | a0001c0001t0001g0075 a0001c0001t0001g0179 a0001c0001t0001g0190 others(5): Show |
8 | HG01255.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-15989_298-1596 others(32): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(23): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0370 a0001c0001t0002g0073 |
3 | HG00639.hp1 HG01934.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.298-15991_298-1596 others(34): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(25): Show |
6 | a0001c0001t0001g0321 a0001c0001t0001g0384 a0001c0001t0002g0026 others(3): Show |
6 | HG02148.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-15962_298-1596 others(36): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTCTCT others(27): Show |
2 | a0001c0001t0001g0053 a0001c0001t0003g0011 |
2 | HG00099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.298-15962_298-1596 others(38): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848239 | T | TTCTTCTC others(6): Show |
1 | a0001c0001t0001g0356 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.298-15990_298-1598 others(17): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848239 | ||||||
| chr3:189848240 | T | C | 70 | a0001c0001t0001g0087 a0001c0001t0001g0153 a0001c0001t0001g0159 others(67): Show |
71 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.298-15992T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848240 | |||||||
| chr3:189848241 | C | CT | 69 | a0001c0001t0001g0087 a0001c0001t0001g0153 a0001c0001t0001g0159 others(66): Show |
70 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.298-15990dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848241 | ||||||
| chr3:189848251 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0002g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.298-15962_298-1596 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848251 | ||||||
| chr3:189848251 | C | CTCTCTCT others(13): Show |
4 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00733.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-15979_298-1596 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848251 | ||||||
| chr3:189848311 | T | G | 91 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0080 others(88): Show |
91 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.298-15921T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848311 | |||||||
| chr3:189848381 | CT | C | 93 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0080 others(90): Show |
93 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.298-15839delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189848381 | ||||||
| chr3:189848408 | A | C | 17 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0274 others(14): Show |
17 | HG00639.hp2 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.298-15824A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848408 | |||||||
| chr3:189848410 | A | T | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-15822A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848410 | |||||||
| chr3:189848458 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298-15774A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189848458 | |||||||
| chr3:189849016 | C | G | 17 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0274 others(14): Show |
17 | HG00639.hp2 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.298-15216C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849016 | |||||||
| chr3:189849055 | C | A | 3 | a0001c0001t0002g0222 a0001c0001t0003g0318 a0001c0001t0003g0341 |
3 | HG01433.hp2 HG04184.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.298-15177C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849055 | |||||||
| chr3:189849569 | A | G | 3 | a0001c0001t0023g0102 a0001c0001t0040g0348 a0001c0003t0004g0304 |
3 | HG02896.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.298-14663A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849569 | |||||||
| chr3:189849721 | A | G | 1 | a0001c0001t0008g0313 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.298-14511A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849721 | |||||||
| chr3:189849757 | A | C | 2 | a0001c0001t0001g0206 a0001c0001t0017g0160 |
2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.298-14475A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849757 | |||||||
| chr3:189849765 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.298-14467C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849765 | |||||||
| chr3:189849806 | T | C | 30 | a0001c0001t0001g0099 a0001c0001t0001g0356 a0001c0001t0001g0357 others(27): Show |
30 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.298-14426T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849806 | |||||||
| chr3:189849946 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0192 |
2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.298-14286G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189849946 | |||||||
| chr3:189850029 | G | C | 323 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0050 others(320): Show |
325 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.298-14203G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850029 | |||||||
| chr3:189850093 | C | T | 129 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.298-14139C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850093 | |||||||
| chr3:189850095 | A | C | 1 | a0001c0001t0011g0386 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298-14137A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850095 | |||||||
| chr3:189850154 | C | T | 1 | a0001c0001t0041g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.298-14078C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850154 | |||||||
| chr3:189850169 | CT | C | 41 | a0001c0001t0001g0064 a0001c0001t0001g0193 a0001c0001t0002g0182 others(38): Show |
41 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.298-14062delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850169 | |||||||
| chr3:189850220 | T | C | 3 | a0001c0001t0006g0078 a0001c0001t0025g0025 a0001c0001t0025g0041 |
3 | HG01255.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.298-14012T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850220 | |||||||
| chr3:189850331 | C | T | 1 | a0001c0001t0005g0361 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.298-13901C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850331 | |||||||
| chr3:189850460 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.298-13772C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850460 | |||||||
| chr3:189850482 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.298-13750A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850482 | |||||||
| chr3:189850591 | C | T | 8 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(5): Show |
8 | HG02523.hp2 HG03239.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-13641C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850591 | |||||||
| chr3:189850652 | C | T | 1 | a0001c0001t0017g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298-13580C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850652 | |||||||
| chr3:189850720 | A | C | 1 | a0001c0001t0003g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298-13512A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850720 | |||||||
| chr3:189850816 | A | C | 3 | a0001c0001t0011g0390 a0001c0001t0011g0391 a0001c0001t0022g0309 |
3 | HG02895.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.298-13416A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189850816 | |||||||
| chr3:189851001 | A | G | 1 | a0001c0001t0003g0395 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298-13231A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851001 | |||||||
| chr3:189851015 | A | G | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-13217A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851015 | |||||||
| chr3:189851043 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.298-13189A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851043 | |||||||
| chr3:189851117 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.298-13115T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851117 | |||||||
| chr3:189851285 | G | A | 3 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0249 |
3 | NA18952.hp2 NA18980.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.298-12947G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851285 | |||||||
| chr3:189851350 | A | G | 8 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(5): Show |
8 | HG02523.hp2 HG03239.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-12882A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851350 | |||||||
| chr3:189851389 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0153 |
2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.298-12843C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851389 | |||||||
| chr3:189851442 | G | C | 1 | a0001c0001t0004g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.298-12790G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851442 | |||||||
| chr3:189851516 | C | T | 3 | a0001c0001t0003g0219 a0001c0001t0003g0224 a0001c0001t0043g0223 |
3 | HG01257.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.298-12716C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851516 | |||||||
| chr3:189851532 | G | A | 72 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0153 others(69): Show |
73 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.298-12700G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851532 | |||||||
| chr3:189851550 | G | A | 4 | a0001c0001t0003g0358 a0001c0001t0011g0076 a0001c0001t0011g0386 others(1): Show |
4 | HG02818.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-12682G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851550 | |||||||
| chr3:189851691 | G | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-12541G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851691 | |||||||
| chr3:189851732 | C | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-12500C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851732 | |||||||
| chr3:189851764 | A | C | 1 | a0001c0001t0003g0395 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298-12468A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851764 | |||||||
| chr3:189851812 | G | T | 8 | a0001c0001t0005g0139 a0001c0001t0005g0161 a0001c0001t0005g0163 others(5): Show |
8 | HG02083.hp1 NA18612.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-12420G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851812 | |||||||
| chr3:189851937 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0002g0282 a0001c0001t0044g0176 |
3 | HG00738.hp2 HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.298-12295C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189851937 | |||||||
| chr3:189852056 | G | A | 37 | a0001c0001t0001g0064 a0001c0001t0001g0081 a0001c0001t0001g0193 others(34): Show |
37 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.298-12176G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852056 | |||||||
| chr3:189852067 | A | G | 42 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(39): Show |
42 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.298-12165A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852067 | |||||||
| chr3:189852092 | G | C | 3 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 |
3 | HG00639.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.298-12140G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852092 | |||||||
| chr3:189852267 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298-11965T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852267 | |||||||
| chr3:189852323 | C | T | 41 | a0001c0001t0001g0064 a0001c0001t0001g0193 a0001c0001t0002g0182 others(38): Show |
41 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.298-11909C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852323 | |||||||
| chr3:189852434 | G | C | 1 | a0001c0001t0044g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-11798G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852434 | |||||||
| chr3:189852567 | T | G | 168 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(165): Show |
169 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.298-11665T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852567 | |||||||
| chr3:189852763 | C | T | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-11469C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852763 | |||||||
| chr3:189852841 | T | C | 121 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(118): Show |
122 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.298-11391T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852841 | |||||||
| chr3:189852923 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0298 a0001c0001t0002g0024 |
3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.298-11309A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189852923 | |||||||
| chr3:189853027 | C | T | 1 | a0001c0001t0005g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.298-11205C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853027 | |||||||
| chr3:189853071 | T | C | 6 | a0001c0001t0005g0089 a0001c0001t0006g0004 a0001c0001t0006g0005 others(3): Show |
6 | HG01243.hp2 HG03490.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-11161T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853071 | |||||||
| chr3:189853155 | G | A | 10 | a0001c0001t0001g0119 a0001c0001t0001g0320 a0001c0001t0001g0363 others(7): Show |
10 | HG00544.hp1 HG01993.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-11077G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853155 | |||||||
| chr3:189853201 | G | T | 6 | a0001c0001t0005g0139 a0001c0001t0005g0161 a0001c0001t0005g0163 others(3): Show |
6 | NA18612.hp1 NA18947.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-11031G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853201 | |||||||
| chr3:189853416 | T | C | 9 | a0001c0001t0039g0232 a0001c0002t0001g0061 a0001c0002t0001g0198 others(6): Show |
9 | HG02523.hp2 HG03239.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-10816T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853416 | |||||||
| chr3:189853859 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.298-10373C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189853859 | |||||||
| chr3:189853965 | A | AT | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-10260dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189853965 | ||||||
| chr3:189854237 | T | A | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.298-9995T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854237 | |||||||
| chr3:189854374 | A | G | 117 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(114): Show |
118 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.298-9858A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854374 | |||||||
| chr3:189854524 | C | T | 7 | a0001c0001t0001g0357 a0001c0001t0002g0258 a0001c0001t0003g0362 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-9708C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854524 | |||||||
| chr3:189854714 | C | G | 20 | a0001c0001t0002g0182 a0001c0001t0002g0208 a0001c0001t0002g0209 others(17): Show |
20 | HG01243.hp2 HG02083.hp1 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-9518C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854714 | |||||||
| chr3:189854725 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.298-9507G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854725 | |||||||
| chr3:189854740 | G | A | 20 | a0001c0001t0002g0182 a0001c0001t0002g0208 a0001c0001t0002g0209 others(17): Show |
20 | HG01243.hp2 HG02083.hp1 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-9492G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854740 | |||||||
| chr3:189854879 | G | A | 77 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(74): Show |
77 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.298-9353G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189854879 | |||||||
| chr3:189855009 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.298-9223G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855009 | |||||||
| chr3:189855116 | C | T | 4 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(1): Show |
4 | NA19010.hp2 NA19057.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-9116C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855116 | |||||||
| chr3:189855126 | G | A | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-9106G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855126 | |||||||
| chr3:189855242 | C | T | 3 | a0001c0001t0011g0382 a0001c0001t0023g0202 a0001c0001t0028g0310 |
3 | HG01891.hp2 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.298-8990C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855242 | |||||||
| chr3:189855458 | T | A | 1 | a0001c0001t0002g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-8774T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855458 | |||||||
| chr3:189855624 | A | G | 10 | a0001c0001t0039g0232 a0001c0002t0001g0061 a0001c0002t0001g0198 others(7): Show |
10 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-8608A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855624 | |||||||
| chr3:189855628 | C | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-8604C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855628 | |||||||
| chr3:189855700 | A | ATG | 11 | a0001c0001t0013g0201 a0001c0001t0039g0232 a0001c0002t0001g0061 others(8): Show |
11 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-8518_298-8517d others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189855700 | ||||||
| chr3:189855708 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.298-8516_298-8501d others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189855708 | ||||||
| chr3:189855716 | A | G | 10 | a0001c0001t0039g0232 a0001c0002t0001g0061 a0001c0002t0001g0198 others(7): Show |
10 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-8516A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855716 | |||||||
| chr3:189855716 | ATGTATGT others(9): Show |
A | 5 | a0001c0001t0003g0358 a0001c0001t0011g0386 a0001c0001t0011g0390 others(2): Show |
5 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-8509_298-8494d others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189855716 | ||||||
| chr3:189855748 | C | T | 1 | a0001c0001t0003g0249 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.298-8484C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855748 | |||||||
| chr3:189855824 | A | G | 1 | a0001c0001t0005g0361 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.298-8408A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855824 | |||||||
| chr3:189855922 | C | T | 30 | a0001c0001t0002g0182 a0001c0001t0002g0208 a0001c0001t0002g0209 others(27): Show |
30 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.298-8310C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189855922 | |||||||
| chr3:189856139 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.298-8093G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856139 | |||||||
| chr3:189856170 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.298-8062T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856170 | |||||||
| chr3:189856207 | G | C | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-8025G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856207 | |||||||
| chr3:189856297 | C | T | 78 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.298-7935C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856297 | |||||||
| chr3:189856427 | T | C | 78 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.298-7805T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856427 | |||||||
| chr3:189856436 | G | GA | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-7789dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189856436 | ||||||
| chr3:189856451 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.298-7781G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856451 | |||||||
| chr3:189856510 | G | A | 78 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.298-7722G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856510 | |||||||
| chr3:189856628 | T | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-7604T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856628 | |||||||
| chr3:189856658 | C | G | 229 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(226): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.298-7574C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856658 | |||||||
| chr3:189856727 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0008g0323 |
2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.298-7505C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856727 | |||||||
| chr3:189856791 | A | G | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-7441A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856791 | |||||||
| chr3:189856928 | T | G | 72 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(69): Show |
73 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.298-7304T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189856928 | |||||||
| chr3:189857018 | A | T | 1 | a0001c0001t0001g0370 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.298-7214A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857018 | |||||||
| chr3:189857038 | A | G | 179 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(176): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.298-7194A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857038 | |||||||
| chr3:189857045 | A | G | 21 | a0001c0001t0001g0356 a0001c0001t0002g0026 a0001c0001t0002g0274 others(18): Show |
21 | HG01109.hp1 HG01255.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.298-7187A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857045 | |||||||
| chr3:189857349 | C | G | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-6883C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857349 | |||||||
| chr3:189857533 | G | A | 98 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(95): Show |
99 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.298-6699G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857533 | |||||||
| chr3:189857654 | C | T | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-6578C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189857654 | |||||||
| chr3:189858105 | TAAGAAAA others(315): Show |
T | 262 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(259): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.298-6108_298-5787d others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189858105 | ||||||
| chr3:189858201 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.298-6031C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858201 | |||||||
| chr3:189858322 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.298-5910G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858322 | |||||||
| chr3:189858403 | C | CA | 13 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0321 others(10): Show |
13 | HG00423.hp1 HG02148.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-5803dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189858403 | ||||||
| chr3:189858403 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298-5815_298-5803d others(15): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189858403 | ||||||
| chr3:189858486 | A | G | 4 | a0001c0001t0011g0386 a0001c0001t0011g0390 a0001c0001t0011g0391 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-5746A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858486 | |||||||
| chr3:189858548 | G | A | 1 | a0001c0001t0019g0335 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.298-5684G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858548 | |||||||
| chr3:189858608 | C | T | 2 | a0001c0001t0003g0211 a0001c0001t0003g0344 |
2 | HG02300.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.298-5624C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858608 | |||||||
| chr3:189858715 | G | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-5517G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858715 | |||||||
| chr3:189858728 | G | A | 1 | a0001c0001t0013g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.298-5504G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858728 | |||||||
| chr3:189858751 | C | G | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-5481C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858751 | |||||||
| chr3:189858811 | T | G | 149 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0062 others(146): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.298-5421T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858811 | |||||||
| chr3:189858962 | A | T | 1 | a0001c0001t0003g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298-5270A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858962 | |||||||
| chr3:189858965 | G | A | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.298-5267G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189858965 | |||||||
| chr3:189859018 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298-5214A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859018 | |||||||
| chr3:189859119 | T | A | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-5113T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859119 | |||||||
| chr3:189859129 | T | C | 74 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.298-5103T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859129 | |||||||
| chr3:189859202 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298-5030A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859202 | |||||||
| chr3:189859244 | A | T | 2 | a0001c0001t0003g0101 a0001c0001t0046g0169 |
2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.298-4988A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859244 | |||||||
| chr3:189859324 | A | G | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-4908A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859324 | |||||||
| chr3:189859339 | C | T | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-4893C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859339 | |||||||
| chr3:189859344 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298-4888G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859344 | |||||||
| chr3:189859547 | C | T | 98 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(95): Show |
99 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.298-4685C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859547 | |||||||
| chr3:189859647 | T | C | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.298-4585T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859647 | |||||||
| chr3:189859703 | G | A | 1 | a0001c0001t0019g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.298-4529G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859703 | |||||||
| chr3:189859738 | G | A | 1 | a0001c0001t0025g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.298-4494G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859738 | |||||||
| chr3:189859780 | T | C | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-4452T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859780 | |||||||
| chr3:189859848 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.298-4384C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859848 | |||||||
| chr3:189859866 | C | A | 261 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(258): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.298-4366C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189859866 | |||||||
| chr3:189860010 | C | G | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.298-4222C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860010 | |||||||
| chr3:189860030 | A | G | 1 | a0001c0001t0012g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298-4202A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860030 | |||||||
| chr3:189860103 | A | T | 31 | a0001c0001t0002g0182 a0001c0001t0002g0208 a0001c0001t0002g0209 others(28): Show |
31 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.298-4129A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860103 | |||||||
| chr3:189860362 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.298-3870A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860362 | |||||||
| chr3:189860367 | T | A | 1 | a0001c0001t0006g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.298-3865T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860367 | |||||||
| chr3:189860461 | G | A | 73 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.298-3771G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860461 | |||||||
| chr3:189860463 | G | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-3769G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860463 | |||||||
| chr3:189860564 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0036 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-3668A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860564 | |||||||
| chr3:189860577 | G | A | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298-3655G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860577 | |||||||
| chr3:189860677 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.298-3555G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860677 | |||||||
| chr3:189860764 | G | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-3468G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860764 | |||||||
| chr3:189860808 | C | A | 10 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(7): Show |
10 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-3424C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189860808 | |||||||
| chr3:189861000 | T | C | 3 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0034g0280 |
3 | HG02257.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-3232T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861000 | |||||||
| chr3:189861080 | T | G | 6 | a0001c0001t0001g0357 a0001c0001t0001g0385 a0001c0001t0012g0018 others(3): Show |
6 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-3152T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861080 | |||||||
| chr3:189861093 | G | T | 230 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(227): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.298-3139G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861093 | |||||||
| chr3:189861142 | C | CCT | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.298-3089_298-3088d others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189861142 | ||||||
| chr3:189861247 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-2985T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861247 | |||||||
| chr3:189861468 | A | G | 2 | a0001c0001t0004g0123 a0001c0001t0004g0144 |
2 | HG02129.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.298-2764A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861468 | |||||||
| chr3:189861597 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298-2635C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861597 | |||||||
| chr3:189861598 | A | T | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298-2634A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861598 | |||||||
| chr3:189861615 | C | T | 1 | a0001c0001t0003g0395 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298-2617C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861615 | |||||||
| chr3:189861652 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.298-2580G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861652 | |||||||
| chr3:189861722 | G | A | 230 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(227): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.298-2510G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861722 | |||||||
| chr3:189861797 | G | A | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-2435G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861797 | |||||||
| chr3:189861809 | A | G | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-2423A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861809 | |||||||
| chr3:189861920 | T | C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0196 a0001c0001t0003g0362 |
3 | HG02602.hp2 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.298-2312T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861920 | |||||||
| chr3:189861930 | C | G | 98 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(95): Show |
99 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.298-2302C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189861930 | |||||||
| chr3:189862050 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-2182G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862050 | |||||||
| chr3:189862058 | T | G | 8 | a0001c0001t0001g0357 a0001c0001t0002g0024 a0001c0001t0012g0018 others(5): Show |
8 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-2174T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862058 | |||||||
| chr3:189862082 | G | A | 1 | a0001c0001t0016g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-2150G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862082 | |||||||
| chr3:189862143 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0033g0291 a0001c0001t0038g0033 |
3 | HG02145.hp2 HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.298-2089A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862143 | |||||||
| chr3:189862299 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-1933G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862299 | |||||||
| chr3:189862308 | A | G | 4 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1924A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862308 | |||||||
| chr3:189862361 | G | A | 1 | a0001c0002t0009g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.298-1871G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862361 | |||||||
| chr3:189862378 | A | G | 4 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1854A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862378 | |||||||
| chr3:189862433 | G | A | 1 | a0001c0001t0002g0336 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.298-1799G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862433 | |||||||
| chr3:189862477 | T | C | 1 | a0001c0001t0012g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.298-1755T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862477 | |||||||
| chr3:189862490 | C | T | 1 | a0001c0001t0040g0348 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.298-1742C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862490 | |||||||
| chr3:189862518 | A | G | 6 | a0001c0001t0003g0358 a0001c0001t0011g0076 a0001c0001t0011g0386 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-1714A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862518 | |||||||
| chr3:189862532 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.298-1700G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862532 | |||||||
| chr3:189862601 | C | G | 1 | a0001c0001t0038g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.298-1631C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862601 | |||||||
| chr3:189862617 | T | C | 73 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.298-1615T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862617 | |||||||
| chr3:189862631 | G | A | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-1601G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862631 | |||||||
| chr3:189862655 | C | T | 1 | a0001c0001t0008g0308 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.298-1577C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862655 | |||||||
| chr3:189862656 | G | A | 4 | a0001c0001t0002g0350 a0001c0001t0023g0102 a0001c0003t0001g0305 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-1576G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862656 | |||||||
| chr3:189862777 | A | G | 12 | a0001c0001t0002g0026 a0001c0001t0002g0274 a0001c0001t0004g0393 others(9): Show |
12 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-1455A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862777 | |||||||
| chr3:189862783 | T | C | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1449T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862783 | |||||||
| chr3:189862866 | C | T | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-1366C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862866 | |||||||
| chr3:189862886 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.298-1346G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862886 | |||||||
| chr3:189862950 | G | A | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-1282G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189862950 | |||||||
| chr3:189863004 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.298-1228A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863004 | |||||||
| chr3:189863094 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 |
3 | HG00639.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.298-1138G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863094 | |||||||
| chr3:189863204 | A | G | 231 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(228): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.298-1028A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863204 | |||||||
| chr3:189863216 | G | GC | 11 | a0001c0001t0002g0225 a0001c0001t0007g0006 a0001c0001t0007g0283 others(8): Show |
11 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-1012dupC | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189863216 | ||||||
| chr3:189863216 | G | T | 107 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(104): Show |
108 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.298-1016G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863216 | |||||||
| chr3:189863231 | A | G | 116 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.298-1001A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863231 | |||||||
| chr3:189863246 | T | C | 1 | a0001c0001t0006g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.298-986T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863246 | |||||||
| chr3:189863255 | T | C | 1 | a0001c0001t0004g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.298-977T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863255 | |||||||
| chr3:189863403 | G | T | 73 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.298-829G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863403 | |||||||
| chr3:189863565 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-667T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863565 | |||||||
| chr3:189863576 | G | C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0196 a0001c0001t0003g0362 |
3 | HG02602.hp2 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.298-656G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863576 | |||||||
| chr3:189863579 | C | T | 1 | a0001c0001t0034g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-653C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863579 | |||||||
| chr3:189863603 | A | G | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-629A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863603 | |||||||
| chr3:189863705 | G | A | 114 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(111): Show |
115 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.298-527G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863705 | |||||||
| chr3:189863746 | TA | T | 262 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(259): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.298-478delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 189863746 | ||||||
| chr3:189863781 | G | C | 115 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(112): Show |
116 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.298-451G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863781 | |||||||
| chr3:189863838 | G | A | 5 | a0001c0001t0004g0057 a0001c0001t0004g0392 a0001c0001t0013g0103 others(2): Show |
5 | HG01081.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-394G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863838 | |||||||
| chr3:189863916 | G | A | 1 | a0001c0001t0001g0376 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.298-316G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189863916 | |||||||
| chr3:189864001 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-231T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189864001 | |||||||
| chr3:189864027 | A | G | 1 | a0001c0001t0012g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298-205A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189864027 | |||||||
| chr3:189864221 | A | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0039 |
3 | HG02055.hp1 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.298-11A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 2/11 | chr3 | 189864221 | |||||||
| chr3:189864452 | T | G | 12 | a0001c0001t0001g0312 a0001c0001t0002g0172 a0001c0001t0002g0222 others(9): Show |
13 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.484+34T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864452 | |||||||
| chr3:189864460 | G | A | 99 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(96): Show |
100 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.484+42G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864460 | |||||||
| chr3:189864541 | C | CT | 17 | a0001c0001t0001g0055 a0001c0001t0001g0117 a0001c0001t0001g0140 others(14): Show |
17 | HG00408.hp1 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+147dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189864541 | ||||||
| chr3:189864541 | CT | C | 167 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0087 others(164): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.484+147delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189864541 | ||||||
| chr3:189864541 | CTT | C | 6 | a0001c0001t0001g0099 a0001c0001t0002g0024 a0001c0001t0002g0040 others(3): Show |
6 | HG00639.hp2 HG02965.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.484+146_484+147del others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189864541 | ||||||
| chr3:189864541 | CTTT | C | 19 | a0001c0001t0001g0357 a0001c0001t0003g0358 a0001c0001t0011g0386 others(16): Show |
19 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.484+145_484+147del others(3): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189864541 | ||||||
| chr3:189864712 | A | G | 11 | a0001c0001t0002g0225 a0001c0001t0007g0006 a0001c0001t0007g0283 others(8): Show |
11 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.484+294A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864712 | |||||||
| chr3:189864728 | T | C | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(36): Show |
39 | HG00408.hp1 HG00544.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.484+310T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864728 | |||||||
| chr3:189864812 | C | A | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+394C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864812 | |||||||
| chr3:189864837 | T | A | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.484+419T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864837 | |||||||
| chr3:189864863 | T | G | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+445T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864863 | |||||||
| chr3:189864875 | C | T | 118 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(115): Show |
119 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.484+457C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864875 | |||||||
| chr3:189864986 | G | A | 1 | a0001c0001t0017g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.484+568G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864986 | |||||||
| chr3:189864993 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.484+575C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189864993 | |||||||
| chr3:189865024 | GA | G | 118 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(115): Show |
119 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.484+615delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189865024 | ||||||
| chr3:189865091 | C | A | 4 | a0001c0001t0001g0099 a0001c0001t0002g0040 a0001c0001t0002g0294 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+673C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865091 | |||||||
| chr3:189865188 | A | T | 1 | a0001c0001t0003g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.484+770A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865188 | |||||||
| chr3:189865193 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0122 |
2 | HG00423.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.484+775C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865193 | |||||||
| chr3:189865203 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.484+785A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865203 | |||||||
| chr3:189865204 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0190 a0001c0001t0002g0375 others(2): Show |
5 | NA18965.hp2 NA18971.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+786A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865204 | |||||||
| chr3:189865299 | G | A | 71 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(68): Show |
72 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.484+881G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865299 | |||||||
| chr3:189865356 | G | A | 2 | a0001c0001t0003g0211 a0001c0001t0003g0344 |
2 | HG02300.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.484+938G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865356 | |||||||
| chr3:189865509 | A | G | 73 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.484+1091A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865509 | |||||||
| chr3:189865728 | A | G | 4 | a0001c0001t0003g0133 a0001c0001t0003g0250 a0001c0001t0003g0267 others(1): Show |
4 | HG00621.hp2 HG02523.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-954A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865728 | |||||||
| chr3:189865870 | C | T | 5 | a0001c0001t0001g0357 a0001c0001t0012g0018 a0001c0001t0012g0019 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-812C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865870 | |||||||
| chr3:189865916 | T | C | 188 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.485-766T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865916 | |||||||
| chr3:189865988 | T | C | 12 | a0001c0001t0002g0026 a0001c0001t0002g0274 a0001c0001t0004g0393 others(9): Show |
12 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.485-694T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189865988 | |||||||
| chr3:189866039 | ATCT | A | 3 | a0001c0001t0001g0356 a0001c0001t0018g0070 a0001c0001t0029g0048 |
3 | HG01109.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.485-638_485-636del others(3): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 189866039 | ||||||
| chr3:189866344 | A | G | 232 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(229): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.485-338A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189866344 | |||||||
| chr3:189866349 | C | T | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-333C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189866349 | |||||||
| chr3:189866376 | G | A | 1 | a0001c0001t0040g0348 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.485-306G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189866376 | |||||||
| chr3:189866604 | C | T | 1 | a0001c0001t0023g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.485-78C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 3/11 | chr3 | 189866604 | |||||||
| chr3:189866813 | C | A | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | NA19010.hp2 NA19057.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.600+16C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189866813 | |||||||
| chr3:189866882 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.600+85G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189866882 | |||||||
| chr3:189866915 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.600+118C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189866915 | |||||||
| chr3:189866958 | C | T | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.600+161C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189866958 | |||||||
| chr3:189867101 | G | A | 368 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0052 others(365): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.600+304G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867101 | |||||||
| chr3:189867118 | T | G | 9 | a0001c0002t0001g0061 a0001c0002t0001g0198 a0001c0002t0002g0259 others(6): Show |
9 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.600+321T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867118 | |||||||
| chr3:189867289 | C | A | 21 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0138 others(18): Show |
21 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.600+492C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867289 | |||||||
| chr3:189867307 | G | A | 1 | a0001c0001t0041g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.600+510G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867307 | |||||||
| chr3:189867343 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601-490C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867343 | |||||||
| chr3:189867419 | A | G | 245 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0062 others(242): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.601-414A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867419 | |||||||
| chr3:189867626 | G | A | 1 | a0001c0001t0017g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.601-207G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867626 | |||||||
| chr3:189867694 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0226 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.601-139A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867694 | |||||||
| chr3:189867745 | G | C | 4 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0295 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-88G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867745 | |||||||
| chr3:189867769 | A | G | 6 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(3): Show |
6 | HG00639.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-64A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 4/11 | chr3 | 189867769 | |||||||
| chr3:189868063 | C | T | 114 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(111): Show |
115 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.710+121C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 5/11 | chr3 | 189868063 | |||||||
| chr3:189868081 | C | T | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.710+139C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 5/11 | chr3 | 189868081 | |||||||
| chr3:189868241 | T | G | 188 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.710+299T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 5/11 | chr3 | 189868241 | |||||||
| chr3:189868393 | A | G | 68 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.711-187A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 5/11 | chr3 | 189868393 | |||||||
| chr3:189868806 | A | T | 1 | a0001c0001t0001g0385 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.847+90A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189868806 | |||||||
| chr3:189868841 | C | G | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.847+125C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189868841 | |||||||
| chr3:189868918 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.847+202A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189868918 | |||||||
| chr3:189869011 | T | TA | 68 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.847+296dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 189869011 | ||||||
| chr3:189869014 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.847+298G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869014 | |||||||
| chr3:189869041 | A | G | 4 | a0001c0001t0012g0010 a0001c0001t0012g0018 a0001c0001t0012g0019 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-283A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869041 | |||||||
| chr3:189869086 | C | A | 1 | a0001c0001t0004g0393 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848-238C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869086 | |||||||
| chr3:189869087 | T | C | 264 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(261): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.848-237T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869087 | |||||||
| chr3:189869126 | A | T | 1 | a0001c0001t0047g0235 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.848-198A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869126 | |||||||
| chr3:189869302 | A | G | 120 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(117): Show |
121 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.848-22A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 6/11 | chr3 | 189869302 | |||||||
| chr3:189869485 | A | G | 206 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(203): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.930+79A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869485 | |||||||
| chr3:189869717 | G | GT | 14 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0138 others(11): Show |
14 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.930+325dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189869717 | ||||||
| chr3:189869729 | T | A | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+323T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869729 | |||||||
| chr3:189869730 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.930+324T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869730 | |||||||
| chr3:189869733 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.930+327T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869733 | |||||||
| chr3:189869736 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.930+330G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869736 | |||||||
| chr3:189869754 | G | A | 2 | a0001c0001t0002g0332 a0001c0001t0021g0337 |
2 | HG01261.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.930+348G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869754 | |||||||
| chr3:189869786 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.930+380C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869786 | |||||||
| chr3:189869825 | A | C | 2 | a0001c0001t0018g0070 a0001c0001t0029g0048 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.930+419A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869825 | |||||||
| chr3:189869871 | A | G | 2 | a0001c0001t0005g0158 a0001c0001t0005g0166 |
2 | HG02015.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.930+465A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869871 | |||||||
| chr3:189869921 | A | G | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+515A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869921 | |||||||
| chr3:189869930 | T | G | 5 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 others(2): Show |
5 | HG02135.hp1 HG02523.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+524T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189869930 | |||||||
| chr3:189869953 | TTCTC | T | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0136 others(3): Show |
6 | NA18947.hp2 NA18977.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+550_930+553del others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189869953 | ||||||
| chr3:189870111 | T | C | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.930+705T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870111 | |||||||
| chr3:189870116 | A | G | 2 | a0001c0001t0001g0326 a0001c0001t0001g0328 |
2 | NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.930+710A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870116 | |||||||
| chr3:189870135 | A | G | 1 | a0001c0001t0032g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.930+729A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870135 | |||||||
| chr3:189870160 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.930+754T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870160 | |||||||
| chr3:189870163 | A | G | 5 | a0001c0001t0002g0225 a0001c0001t0020g0284 a0001c0001t0020g0330 others(2): Show |
5 | HG01433.hp1 HG01978.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+757A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870163 | |||||||
| chr3:189870197 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.930+791T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870197 | |||||||
| chr3:189870261 | A | C | 182 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(179): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.930+855A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870261 | |||||||
| chr3:189870587 | G | A | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.930+1181G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870587 | |||||||
| chr3:189870630 | G | C | 1 | a0001c0001t0044g0176 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.930+1224G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870630 | |||||||
| chr3:189870758 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.930+1352A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870758 | |||||||
| chr3:189870759 | A | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0264 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.930+1353A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870759 | |||||||
| chr3:189870802 | C | T | 1 | a0001c0001t0004g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.930+1396C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189870802 | |||||||
| chr3:189871258 | G | A | 69 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0153 others(66): Show |
70 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.931-1601G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871258 | |||||||
| chr3:189871266 | C | T | 69 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0153 others(66): Show |
70 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.931-1593C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871266 | |||||||
| chr3:189871625 | G | A | 2 | a0001c0001t0003g0211 a0001c0001t0003g0344 |
2 | HG02300.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.931-1234G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871625 | |||||||
| chr3:189871712 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.931-1147A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871712 | |||||||
| chr3:189871869 | G | A | 1 | a0001c0001t0047g0235 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.931-990G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871869 | |||||||
| chr3:189871878 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0001g0328 |
2 | NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.931-981C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871878 | |||||||
| chr3:189871951 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.931-908G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189871951 | |||||||
| chr3:189872027 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.931-832G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872027 | |||||||
| chr3:189872050 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.931-809G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872050 | |||||||
| chr3:189872264 | A | AT | 363 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0055 others(360): Show |
365 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.931-595_931-594ins others(1): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872264 | |||||||
| chr3:189872372 | A | G | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.931-487A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872372 | |||||||
| chr3:189872400 | A | AAC | 60 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.931-427_931-426dup others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | A | AACAC | 5 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0385 others(2): Show |
5 | HG02300.hp2 HG03041.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-429_931-426dup others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | A | AACACACA others(1): Show |
5 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(2): Show |
5 | HG02135.hp1 HG02523.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-433_931-426dup others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | A | AACACACA others(3): Show |
2 | a0001c0001t0002g0024 a0001c0002t0009g0086 |
2 | HG02965.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.931-435_931-426dup others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | AAC | A | 21 | a0001c0001t0002g0042 a0001c0001t0002g0293 a0001c0001t0002g0350 others(18): Show |
21 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.931-427_931-426del others(2): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | AACAC | A | 117 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0099 others(114): Show |
118 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.931-429_931-426del others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | AACACACA others(1): Show |
A | 7 | a0001c0001t0011g0076 a0001c0001t0011g0382 a0001c0001t0011g0386 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.931-433_931-426del others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872400 | AACACACA others(3): Show |
A | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.931-435_931-426del others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 189872400 | ||||||
| chr3:189872434 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.931-425T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872434 | |||||||
| chr3:189872544 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.931-315C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872544 | |||||||
| chr3:189872565 | G | A | 1 | a0001c0001t0031g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.931-294G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872565 | |||||||
| chr3:189872588 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.931-271G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872588 | |||||||
| chr3:189872610 | A | G | 1 | a0001c0001t0003g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.931-249A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872610 | |||||||
| chr3:189872771 | G | A | 1 | a0001c0001t0003g0358 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.931-88G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 7/11 | chr3 | 189872771 | |||||||
| chr3:189873010 | G | A | 1 | a0001c0001t0006g0252 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1067+15G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873010 | |||||||
| chr3:189873035 | G | C | 188 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0081 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1067+40G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873035 | |||||||
| chr3:189873036 | G | A | 99 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(96): Show |
100 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.1067+41G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873036 | |||||||
| chr3:189873061 | G | A | 2 | a0001c0001t0005g0327 a0001c0001t0006g0100 |
2 | NA19001.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1067+66G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873061 | |||||||
| chr3:189873082 | G | A | 23 | a0001c0001t0005g0089 a0001c0001t0005g0110 a0001c0001t0005g0139 others(20): Show |
23 | HG01243.hp2 HG01255.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1067+87G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873082 | |||||||
| chr3:189873096 | A | G | 1 | a0001c0001t0002g0287 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1067+101A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873096 | |||||||
| chr3:189873264 | G | T | 364 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0055 others(361): Show |
366 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.1067+269G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873264 | |||||||
| chr3:189873504 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1067+509C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873504 | |||||||
| chr3:189873568 | A | C | 195 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0081 others(192): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1067+573A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873568 | |||||||
| chr3:189873670 | G | C | 90 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(87): Show |
90 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1067+675G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873670 | |||||||
| chr3:189873861 | T | C | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+866T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873861 | |||||||
| chr3:189873991 | A | T | 69 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0064 others(66): Show |
69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1067+996A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189873991 | |||||||
| chr3:189874048 | G | A | 3 | a0001c0001t0013g0103 a0001c0001t0013g0201 a0001c0001t0013g0383 |
3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1067+1053G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874048 | |||||||
| chr3:189874162 | C | T | 9 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(6): Show |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+1167C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874162 | |||||||
| chr3:189874209 | A | T | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1067+1214A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874209 | |||||||
| chr3:189874289 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1067+1294C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874289 | |||||||
| chr3:189874413 | A | G | 189 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(186): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1067+1418A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874413 | |||||||
| chr3:189874462 | A | G | 1 | a0001c0001t0005g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1067+1467A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874462 | |||||||
| chr3:189874533 | C | T | 5 | a0001c0001t0017g0032 a0001c0001t0020g0284 a0001c0001t0020g0330 others(2): Show |
5 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+1538C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874533 | |||||||
| chr3:189874534 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0039 |
3 | HG02055.hp1 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1067+1539G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874534 | |||||||
| chr3:189874822 | A | G | 3 | a0001c0001t0013g0103 a0001c0001t0013g0201 a0001c0001t0013g0383 |
3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1067+1827A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874822 | |||||||
| chr3:189874865 | T | C | 195 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(192): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1067+1870T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874865 | |||||||
| chr3:189874939 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1067+1944T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189874939 | |||||||
| chr3:189874981 | C | CT | 6 | a0001c0001t0001g0314 a0001c0001t0001g0366 a0001c0001t0002g0230 others(3): Show |
6 | HG00597.hp1 HG00609.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+2005dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189874981 | ||||||
| chr3:189874981 | CT | C | 59 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(56): Show |
59 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1067+2005delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189874981 | ||||||
| chr3:189874981 | CTTTTT | C | 26 | a0001c0001t0005g0089 a0001c0001t0005g0110 a0001c0001t0005g0139 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1067+2001_1067+200 others(9): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189874981 | ||||||
| chr3:189875089 | G | T | 15 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0299 others(12): Show |
15 | HG02145.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1067+2094G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875089 | |||||||
| chr3:189875301 | C | T | 1 | a0001c0001t0019g0335 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1067+2306C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875301 | |||||||
| chr3:189875398 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1067+2403G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875398 | |||||||
| chr3:189875428 | A | T | 186 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(183): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1067+2433A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875428 | |||||||
| chr3:189875528 | T | TGCAC | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1067+2534_1067+253 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875528 | ||||||
| chr3:189875585 | A | AATACATA others(7): Show |
3 | a0001c0001t0002g0175 a0001c0001t0002g0266 a0001c0001t0019g0174 |
3 | HG00408.hp1 HG01261.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875585 | ||||||
| chr3:189875589 | C | CAT | 13 | a0001c0001t0003g0020 a0001c0001t0003g0035 a0001c0001t0003g0047 others(10): Show |
13 | HG01257.hp1 HG01517.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067+2596_1067+259 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATAT | 13 | a0001c0001t0003g0028 a0001c0001t0003g0121 a0001c0001t0003g0181 others(10): Show |
13 | HG00621.hp2 HG02293.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATACA others(5): Show |
2 | a0001c0001t0002g0069 a0001c0001t0030g0066 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATACA others(13): Show |
1 | a0001c0001t0002g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1067+2597_1067+259 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATAT | 5 | a0001c0001t0003g0212 a0001c0001t0003g0351 a0001c0001t0004g0392 others(2): Show |
5 | HG00741.hp1 HG03471.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(1): Show |
13 | a0001c0001t0003g0014 a0001c0001t0003g0039 a0001c0001t0003g0068 others(10): Show |
13 | HG02083.hp1 HG02109.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(12): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(3): Show |
21 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0388 others(18): Show |
21 | HG01934.hp2 HG02055.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(5): Show |
9 | a0001c0001t0001g0087 a0001c0001t0003g0011 a0001c0001t0003g0030 others(6): Show |
9 | HG00423.hp2 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(9): Show |
2 | a0001c0001t0001g0152 a0001c0001t0019g0335 |
2 | HG01358.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(11): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0178 a0001c0001t0001g0360 |
3 | HG00438.hp1 HG02155.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(7): Show |
2 | a0001c0001t0004g0207 a0001c0001t0005g0158 |
2 | NA18747.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(9): Show |
3 | a0001c0001t0005g0163 a0001c0001t0022g0325 a0001c0002t0009g0142 |
3 | HG02135.hp1 HG02970.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | C | CATATATA others(15): Show |
1 | a0001c0001t0002g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1067+2597_1067+259 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(1): Show |
C | 4 | a0001c0001t0003g0249 a0001c0001t0003g0378 a0001c0001t0004g0171 others(1): Show |
4 | HG03490.hp2 NA18953.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+2598_1067+260 others(12): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(3): Show |
C | 6 | a0001c0001t0003g0104 a0001c0001t0003g0211 a0001c0001t0003g0250 others(3): Show |
6 | HG02300.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+2598_1067+260 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(5): Show |
C | 1 | a0001c0001t0005g0327 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1067+2598_1067+260 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(7): Show |
C | 5 | a0001c0001t0010g0067 a0001c0001t0020g0284 a0001c0001t0020g0330 others(2): Show |
5 | HG01891.hp1 HG01978.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+2598_1067+261 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(9): Show |
C | 1 | a0001c0001t0006g0007 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1067+2598_1067+261 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(11): Show |
C | 1 | a0001c0001t0003g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1067+2598_1067+261 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(15): Show |
C | 6 | a0001c0001t0003g0318 a0001c0001t0003g0341 a0001c0001t0004g0095 others(3): Show |
6 | HG00280.hp2 HG01175.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+2598_1067+261 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(17): Show |
C | 4 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 others(1): Show |
4 | HG02523.hp2 NA18939.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+2598_1067+262 others(28): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(19): Show |
C | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1067+2598_1067+262 others(30): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(21): Show |
C | 3 | a0001c0001t0013g0103 a0001c0001t0013g0201 a0001c0001t0013g0383 |
3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1067+2598_1067+262 others(32): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875589 | CATACATA others(23): Show |
C | 1 | a0001c0001t0016g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1067+2598_1067+262 others(34): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875589 | ||||||
| chr3:189875591 | T | TATATATA others(5): Show |
4 | a0001c0001t0002g0208 a0001c0001t0002g0243 a0001c0001t0019g0297 others(1): Show |
4 | HG02056.hp1 HG02615.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+2597_1067+259 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875591 | ||||||
| chr3:189875593 | C | CAT | 29 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0055 others(26): Show |
29 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1067+2642_1067+264 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | CATAT | 26 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0054 others(23): Show |
26 | HG00280.hp1 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1067+2640_1067+264 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | CATATAT | 5 | a0001c0001t0001g0125 a0001c0001t0002g0245 a0001c0001t0002g0302 others(2): Show |
5 | HG00558.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+2638_1067+264 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | CATATATA others(1): Show |
4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0179 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+2636_1067+264 others(12): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0300 |
3 | HG03710.hp2 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1067+2634_1067+264 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | CATATATA others(5): Show |
1 | a0001c0001t0018g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1067+2632_1067+264 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | C | T | 215 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(212): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+2598C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875593 | |||||||
| chr3:189875593 | CAT | C | 17 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0141 others(14): Show |
17 | HG00738.hp2 HG01358.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1067+2642_1067+264 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | CATAT | C | 3 | a0001c0001t0001g0320 a0001c0001t0002g0269 a0001c0001t0029g0048 |
3 | HG01993.hp2 HG03139.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1067+2640_1067+264 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | CATATATA others(9): Show |
C | 4 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(1): Show |
4 | NA19010.hp2 NA19057.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2628_1067+264 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875593 | CATATATA others(21): Show |
C | 2 | a0001c0001t0001g0120 a0001c0001t0002g0191 |
2 | HG00423.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1067+2616_1067+264 others(32): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875593 | ||||||
| chr3:189875595 | T | TATATATA others(1): Show |
10 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0173 others(7): Show |
10 | HG01069.hp1 HG01109.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1067+2607_1067+260 others(12): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875595 | ||||||
| chr3:189875597 | T | TATATAC | 4 | a0001c0001t0001g0062 a0001c0001t0001g0122 a0001c0001t0002g0016 others(1): Show |
4 | HG03669.hp1 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+2607_1067+260 others(10): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875597 | ||||||
| chr3:189875599 | T | TATAC | 4 | a0001c0001t0001g0063 a0001c0001t0014g0079 a0001c0001t0014g0082 others(1): Show |
4 | HG01070.hp2 HG02148.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2607_1067+260 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875599 | ||||||
| chr3:189875601 | T | TAC | 3 | a0001c0001t0001g0083 a0001c0001t0001g0199 a0001c0001t0002g0263 |
3 | NA18948.hp1 NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1067+2607_1067+260 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875601 | ||||||
| chr3:189875603 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0205 |
2 | HG00544.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1067+2608T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875603 | |||||||
| chr3:189875604 | A | G | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1067+2609A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875604 | |||||||
| chr3:189875605 | T | TATATATA others(9): Show |
1 | a0001c0001t0010g0387 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875605 | ||||||
| chr3:189875605 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875605 | ||||||
| chr3:189875607 | T | TATATATA others(7): Show |
1 | a0001c0001t0002g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875607 | ||||||
| chr3:189875609 | T | TATATATA others(1): Show |
3 | a0001c0001t0012g0010 a0001c0001t0025g0025 a0001c0001t0025g0041 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1067+2621_1067+262 others(12): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(3): Show |
3 | a0001c0001t0010g0098 a0001c0001t0010g0105 a0001c0001t0010g0352 |
3 | HG03041.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1067+2623_1067+262 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(5): Show |
1 | a0001c0001t0026g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(16): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(7): Show |
7 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(4): Show |
7 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+2625_1067+262 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(11): Show |
3 | a0001c0001t0001g0371 a0001c0001t0002g0218 a0001c0001t0002g0251 |
3 | HG00140.hp1 HG00621.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1067+2627_1067+262 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(47): Show |
1 | a0001c0001t0001g0369 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(58): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(11): Show |
2 | a0001c0001t0007g0286 a0001c0001t0007g0342 |
2 | HG01069.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1067+2629_1067+263 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATATA others(13): Show |
2 | a0001c0001t0001g0164 a0001c0001t0008g0306 |
2 | HG01975.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1067+2629_1067+263 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875609 | T | TATATGTA others(13): Show |
1 | a0001c0001t0035g0097 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1067+2618_1067+261 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875609 | ||||||
| chr3:189875611 | T | TATATATA others(29): Show |
1 | a0001c0001t0026g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1067+2623_1067+262 others(40): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(3): Show |
1 | a0001c0001t0010g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(14): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0159 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(9): Show |
17 | a0001c0001t0001g0056 a0001c0001t0001g0112 a0001c0001t0001g0135 others(14): Show |
17 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1067+2627_1067+262 others(20): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(47): Show |
1 | a0001c0001t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(58): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(33): Show |
1 | a0001c0001t0017g0160 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(44): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0206 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(46): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(11): Show |
15 | a0001c0001t0001g0060 a0001c0001t0001g0108 a0001c0001t0001g0111 others(12): Show |
15 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1067+2629_1067+263 others(22): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(13): Show |
3 | a0001c0001t0002g0332 a0001c0001t0003g0003 a0001c0001t0021g0337 |
4 | HG01256.hp1 HG01258.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2631_1067+263 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(15): Show |
7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0136 others(4): Show |
7 | HG01168.hp2 HG02976.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+2633_1067+263 others(26): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875611 | T | TATATATA others(17): Show |
2 | a0001c0001t0002g0276 a0001c0001t0049g0339 |
2 | HG00099.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1067+2635_1067+263 others(28): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875611 | ||||||
| chr3:189875613 | T | TATATATA others(7): Show |
1 | a0001c0001t0021g0338 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1067+2627_1067+262 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875613 | ||||||
| chr3:189875613 | T | TATATATA others(13): Show |
1 | a0001c0001t0002g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1067+2633_1067+263 others(24): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875613 | ||||||
| chr3:189875613 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0385 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1067+2641_1067+264 others(32): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875613 | ||||||
| chr3:189875615 | T | C | 2 | a0001c0001t0002g0294 a0001c0001t0028g0310 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1067+2620T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875615 | |||||||
| chr3:189875615 | T | TAC | 4 | a0001c0001t0011g0382 a0001c0001t0011g0386 a0001c0001t0011g0390 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2621_1067+262 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875615 | ||||||
| chr3:189875615 | T | TATATATA others(41): Show |
2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1067+2627_1067+262 others(52): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875615 | ||||||
| chr3:189875615 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1067+2629_1067+263 others(18): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875615 | ||||||
| chr3:189875616 | A | ACATATAT others(17): Show |
4 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(1): Show |
4 | HG00639.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2621_1067+262 others(28): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875616 | |||||||
| chr3:189875616 | A | ATATACAT others(19): Show |
1 | a0001c0001t0040g0348 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1067+2625_1067+262 others(30): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875616 | ||||||
| chr3:189875616 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1067+2621A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875616 | |||||||
| chr3:189875622 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1067+2627A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875622 | |||||||
| chr3:189875630 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1067+2635A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875630 | |||||||
| chr3:189875637 | T | A | 1 | a0001c0001t0002g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1067+2642T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875637 | |||||||
| chr3:189875638 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1067+2643_1067+264 others(17): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875638 | |||||||
| chr3:189875639 | A | T | 1 | a0001c0001t0001g0389 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1067+2644A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875639 | |||||||
| chr3:189875689 | G | A | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1067+2694G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875689 | |||||||
| chr3:189875746 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1067+2751A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875746 | |||||||
| chr3:189875806 | G | C | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2811G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875806 | |||||||
| chr3:189875840 | AG | A | 248 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(245): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1067+2846delG | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875840 | |||||||
| chr3:189875902 | T | C | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+2907T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875902 | |||||||
| chr3:189875947 | G | C | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+2952G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189875947 | |||||||
| chr3:189875961 | A | AT | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067+2968dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189875961 | ||||||
| chr3:189876348 | G | T | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1067+3353G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189876348 | |||||||
| chr3:189876394 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1067+3399C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189876394 | |||||||
| chr3:189876567 | G | T | 2 | a0001c0001t0005g0158 a0001c0001t0005g0166 |
2 | HG02015.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1067+3572G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189876567 | |||||||
| chr3:189876931 | A | G | 2 | a0001c0001t0002g0218 a0001c0001t0002g0251 |
2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1067+3936A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189876931 | |||||||
| chr3:189877125 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1067+4130C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877125 | |||||||
| chr3:189877371 | G | A | 1 | a0001c0001t0026g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1067+4376G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877371 | |||||||
| chr3:189877423 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0002g0265 |
3 | HG00558.hp2 NA18943.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1067+4428T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877423 | |||||||
| chr3:189877426 | G | A | 128 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(125): Show |
129 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1067+4431G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877426 | |||||||
| chr3:189877491 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1067+4496G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877491 | |||||||
| chr3:189877616 | G | C | 6 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 others(3): Show |
6 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+4621G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877616 | |||||||
| chr3:189877800 | A | G | 1 | a0001c0001t0001g0357 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1067+4805A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877800 | |||||||
| chr3:189877801 | A | G | 1 | a0001c0001t0017g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1067+4806A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877801 | |||||||
| chr3:189877883 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0002g0265 |
3 | HG00558.hp2 NA18943.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1067+4888T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877883 | |||||||
| chr3:189877974 | C | T | 6 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(3): Show |
6 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+4979C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877974 | |||||||
| chr3:189877991 | C | G | 26 | a0001c0001t0005g0089 a0001c0001t0005g0110 a0001c0001t0005g0139 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1067+4996C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189877991 | |||||||
| chr3:189878270 | G | T | 8 | a0001c0001t0010g0067 a0001c0001t0010g0093 a0001c0001t0010g0098 others(5): Show |
8 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1067+5275G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878270 | |||||||
| chr3:189878359 | G | A | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067+5364G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878359 | |||||||
| chr3:189878385 | C | CT | 10 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0002g0216 others(7): Show |
10 | HG00140.hp1 HG01361.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1067+5411dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878385 | ||||||
| chr3:189878385 | CT | C | 116 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0099 others(113): Show |
117 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1067+5411delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878385 | ||||||
| chr3:189878385 | CTT | C | 9 | a0001c0001t0002g0040 a0001c0001t0003g0212 a0001c0001t0004g0392 others(6): Show |
9 | HG01081.hp1 HG02895.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+5410_1067+541 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878385 | ||||||
| chr3:189878409 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1067+5414G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878409 | |||||||
| chr3:189878467 | A | C | 266 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(263): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1067+5472A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878467 | |||||||
| chr3:189878488 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1067+5493G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878488 | |||||||
| chr3:189878501 | G | A | 9 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(6): Show |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+5506G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878501 | |||||||
| chr3:189878516 | G | A | 4 | a0001c0001t0003g0247 a0001c0001t0013g0103 a0001c0001t0013g0201 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+5521G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878516 | |||||||
| chr3:189878532 | A | T | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1067+5537A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878532 | |||||||
| chr3:189878536 | C | T | 9 | a0001c0001t0007g0006 a0001c0001t0007g0283 a0001c0001t0007g0285 others(6): Show |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+5541C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878536 | |||||||
| chr3:189878549 | C | T | 3 | a0001c0001t0013g0103 a0001c0001t0013g0201 a0001c0001t0013g0383 |
3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1067+5554C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878549 | |||||||
| chr3:189878591 | TTC | T | 9 | a0001c0001t0002g0026 a0001c0001t0010g0067 a0001c0001t0010g0093 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+5598_1067+559 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878591 | ||||||
| chr3:189878593 | C | CT | 6 | a0001c0001t0001g0120 a0001c0001t0001g0184 a0001c0001t0002g0132 others(3): Show |
6 | HG00423.hp1 HG00609.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067+5613dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878593 | ||||||
| chr3:189878593 | CT | C | 254 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(251): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1067+5613delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878593 | ||||||
| chr3:189878594 | T | C | 9 | a0001c0001t0002g0026 a0001c0001t0010g0067 a0001c0001t0010g0093 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+5599T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878594 | |||||||
| chr3:189878598 | T | C | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1067+5603T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878598 | |||||||
| chr3:189878635 | G | A | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067+5640G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878635 | |||||||
| chr3:189878673 | CGACCTTG others(193): Show |
C | 81 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0153 others(78): Show |
82 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1067+5813_1067+601 others(4): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189878673 | ||||||
| chr3:189878809 | C | G | 1 | a0001c0001t0002g0271 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1067+5814C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878809 | |||||||
| chr3:189878873 | T | C | 312 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1067+5878T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878873 | |||||||
| chr3:189878918 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1067+5923G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878918 | |||||||
| chr3:189878932 | G | C | 1 | a0001c0001t0013g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1067+5937G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878932 | |||||||
| chr3:189878975 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1067+5980A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189878975 | |||||||
| chr3:189879011 | C | A | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1067+6016C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879011 | |||||||
| chr3:189879051 | A | G | 135 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(132): Show |
136 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1067+6056A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879051 | |||||||
| chr3:189879053 | C | A | 3 | a0001c0001t0013g0103 a0001c0001t0013g0201 a0001c0001t0013g0383 |
3 | HG01081.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1067+6058C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879053 | |||||||
| chr3:189879066 | A | G | 59 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1067+6071A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879066 | |||||||
| chr3:189879142 | C | T | 23 | a0001c0001t0005g0089 a0001c0001t0005g0110 a0001c0001t0005g0139 others(20): Show |
23 | HG01243.hp2 HG01255.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1067+6147C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879142 | |||||||
| chr3:189879523 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1067+6528T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879523 | |||||||
| chr3:189879646 | T | A | 1 | a0001c0001t0002g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1067+6651T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879646 | |||||||
| chr3:189879893 | C | G | 1 | a0001c0001t0018g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1068-6501C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879893 | |||||||
| chr3:189879959 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1068-6435T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189879959 | |||||||
| chr3:189880156 | C | G | 1 | a0001c0002t0009g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1068-6238C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880156 | |||||||
| chr3:189880249 | G | A | 2 | a0001c0001t0001g0355 a0001c0001t0001g0357 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1068-6145G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880249 | |||||||
| chr3:189880337 | G | T | 4 | a0001c0001t0015g0146 a0001c0001t0015g0147 a0001c0001t0015g0148 others(1): Show |
4 | HG00642.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-6057G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880337 | |||||||
| chr3:189880437 | T | G | 1 | a0001c0001t0018g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1068-5957T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880437 | |||||||
| chr3:189880505 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1068-5889G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880505 | |||||||
| chr3:189880555 | A | G | 3 | a0001c0001t0002g0278 a0001c0001t0002g0302 a0001c0001t0002g0303 |
3 | HG00438.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1068-5839A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880555 | |||||||
| chr3:189880635 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1068-5759G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880635 | |||||||
| chr3:189880723 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0002g0009 a0001c0001t0002g0069 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-5671A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880723 | |||||||
| chr3:189880817 | C | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0394 a0001c0001t0002g0349 |
3 | HG03486.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1068-5577C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189880817 | |||||||
| chr3:189881102 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1068-5292G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881102 | |||||||
| chr3:189881113 | C | T | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068-5281C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881113 | |||||||
| chr3:189881123 | A | G | 1 | a0001c0003t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1068-5271A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881123 | |||||||
| chr3:189881131 | T | A | 1 | a0001c0001t0002g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1068-5263T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881131 | |||||||
| chr3:189881181 | T | TA | 49 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(46): Show |
49 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1068-5212dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189881181 | ||||||
| chr3:189881443 | T | C | 1 | a0001c0001t0022g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1068-4951T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881443 | |||||||
| chr3:189881535 | T | C | 195 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(192): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1068-4859T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881535 | |||||||
| chr3:189881728 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1068-4666A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881728 | |||||||
| chr3:189881850 | T | G | 1 | a0001c0001t0006g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1068-4544T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881850 | |||||||
| chr3:189881885 | T | C | 70 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(67): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1068-4509T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189881885 | |||||||
| chr3:189882018 | C | CA | 115 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(112): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1068-4364dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189882018 | ||||||
| chr3:189882018 | C | CAA | 80 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(77): Show |
81 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1068-4365_1068-436 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189882018 | ||||||
| chr3:189882246 | T | A | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-4148T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882246 | |||||||
| chr3:189882371 | A | G | 143 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0062 others(140): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1068-4023A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882371 | |||||||
| chr3:189882436 | A | T | 4 | a0001c0001t0003g0011 a0001c0001t0003g0028 a0001c0001t0003g0068 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-3958A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882436 | |||||||
| chr3:189882464 | C | CT | 61 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0111 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1068-3914dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189882464 | ||||||
| chr3:189882464 | CT | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0002g0189 others(5): Show |
8 | HG01243.hp2 HG01358.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068-3914delT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189882464 | ||||||
| chr3:189882464 | CTT | C | 106 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0087 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.1068-3915_1068-391 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189882464 | ||||||
| chr3:189882518 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1068-3876C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882518 | |||||||
| chr3:189882687 | T | C | 17 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(14): Show |
17 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068-3707T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882687 | |||||||
| chr3:189882730 | A | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0162 a0001c0001t0002g0034 others(1): Show |
4 | HG02155.hp2 NA18747.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-3664A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882730 | |||||||
| chr3:189882908 | C | T | 17 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(14): Show |
17 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068-3486C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882908 | |||||||
| chr3:189882909 | G | A | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-3485G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189882909 | |||||||
| chr3:189883122 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0394 a0001c0001t0002g0349 |
3 | HG03486.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1068-3272C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883122 | |||||||
| chr3:189883183 | A | AT | 194 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1068-3203dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189883183 | ||||||
| chr3:189883191 | T | TA | 46 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1068-3197dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189883191 | ||||||
| chr3:189883257 | C | A | 250 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(247): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1068-3137C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883257 | |||||||
| chr3:189883335 | C | T | 6 | a0001c0001t0001g0356 a0001c0001t0018g0031 a0001c0001t0018g0036 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068-3059C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883335 | |||||||
| chr3:189883376 | T | C | 6 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 others(3): Show |
6 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068-3018T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883376 | |||||||
| chr3:189883545 | G | T | 1 | a0001c0001t0002g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1068-2849G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883545 | |||||||
| chr3:189883592 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1068-2802C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883592 | |||||||
| chr3:189883809 | T | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1068-2585T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883809 | |||||||
| chr3:189883853 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0036 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1068-2541A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883853 | |||||||
| chr3:189883932 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1068-2462G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189883932 | |||||||
| chr3:189883937 | G | GA | 122 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0063 others(119): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1068-2445dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189883937 | ||||||
| chr3:189883937 | GA | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0320 a0001c0001t0001g0363 others(4): Show |
7 | HG01993.hp2 HG02083.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068-2445delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 189883937 | ||||||
| chr3:189884048 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1068-2346G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884048 | |||||||
| chr3:189884116 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1068-2278G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884116 | |||||||
| chr3:189884283 | C | T | 1 | a0001c0001t0002g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1068-2111C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884283 | |||||||
| chr3:189884301 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1068-2093G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884301 | |||||||
| chr3:189884455 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1068-1939C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884455 | |||||||
| chr3:189884501 | C | A | 1 | a0001c0001t0002g0177 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1068-1893C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884501 | |||||||
| chr3:189884502 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0002g0292 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1068-1892A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884502 | |||||||
| chr3:189884610 | C | T | 1 | a0001c0001t0005g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1068-1784C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884610 | |||||||
| chr3:189884611 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0298 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1068-1783G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884611 | |||||||
| chr3:189884918 | AAGAC | A | 4 | a0001c0001t0011g0386 a0001c0001t0011g0390 a0001c0001t0011g0391 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-1475_1068-147 others(8): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884918 | |||||||
| chr3:189884946 | A | C | 14 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0299 others(11): Show |
14 | HG02145.hp1 HG02257.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1068-1448A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884946 | |||||||
| chr3:189884993 | A | G | 1 | a0001c0001t0016g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1068-1401A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189884993 | |||||||
| chr3:189885064 | T | C | 6 | a0001c0001t0002g0222 a0001c0001t0002g0287 a0001c0001t0002g0332 others(3): Show |
6 | HG00099.hp2 HG01168.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068-1330T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885064 | |||||||
| chr3:189885192 | T | C | 7 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0154 others(4): Show |
7 | HG02155.hp2 NA18747.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068-1202T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885192 | |||||||
| chr3:189885217 | G | A | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0038 |
3 | HG01074.hp1 HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1068-1177G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885217 | |||||||
| chr3:189885299 | G | A | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1068-1095G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885299 | |||||||
| chr3:189885422 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1068-972A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885422 | |||||||
| chr3:189885457 | G | T | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-937G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885457 | |||||||
| chr3:189885588 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1068-806G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885588 | |||||||
| chr3:189885630 | A | G | 1 | a0001c0001t0016g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1068-764A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885630 | |||||||
| chr3:189885717 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0017g0160 |
2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1068-677T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885717 | |||||||
| chr3:189885909 | G | C | 172 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(169): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1068-485G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189885909 | |||||||
| chr3:189886007 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0019g0297 |
2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1068-387G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886007 | |||||||
| chr3:189886186 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1068-208G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886186 | |||||||
| chr3:189886332 | A | G | 1 | a0001c0001t0001g0356 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1068-62A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886332 | |||||||
| chr3:189886338 | A | C | 1 | a0001c0001t0007g0286 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1068-56A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886338 | |||||||
| chr3:189886360 | T | G | 270 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(267): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1068-34T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886360 | |||||||
| chr3:189886371 | T | C | 270 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(267): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1068-23T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 8/11 | chr3 | 189886371 | |||||||
| chr3:189886575 | T | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(3): Show |
6 | HG00639.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225+24T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886575 | |||||||
| chr3:189886629 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1225+78T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886629 | |||||||
| chr3:189886815 | C | T | 10 | a0001c0001t0010g0067 a0001c0001t0010g0093 a0001c0001t0010g0098 others(7): Show |
10 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1225+264C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886815 | |||||||
| chr3:189886820 | A | G | 22 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0206 others(19): Show |
22 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1225+269A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886820 | |||||||
| chr3:189886851 | T | C | 2 | a0001c0001t0025g0025 a0001c0001t0025g0041 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1225+300T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886851 | |||||||
| chr3:189886871 | C | T | 3 | a0001c0001t0003g0133 a0001c0001t0003g0250 a0001c0001t0003g0267 |
3 | HG00621.hp2 HG02523.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1225+320C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886871 | |||||||
| chr3:189886982 | G | A | 1 | a0001c0001t0049g0339 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1225+431G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189886982 | |||||||
| chr3:189887037 | C | T | 4 | a0001c0001t0001g0356 a0001c0001t0012g0296 a0001c0001t0033g0291 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+486C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887037 | |||||||
| chr3:189887053 | A | C | 1 | a0001c0001t0002g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1225+502A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887053 | |||||||
| chr3:189887091 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0362 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1225+540C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887091 | |||||||
| chr3:189887138 | G | A | 8 | a0001c0001t0010g0067 a0001c0001t0010g0093 a0001c0001t0010g0098 others(5): Show |
8 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225+587G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887138 | |||||||
| chr3:189887208 | C | CA | 24 | a0001c0001t0001g0075 a0001c0001t0001g0183 a0001c0001t0001g0190 others(21): Show |
24 | HG01070.hp2 HG01109.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1225+674dupA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 189887208 | ||||||
| chr3:189887208 | CA | C | 48 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0134 others(45): Show |
48 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1225+674delA | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 189887208 | ||||||
| chr3:189887361 | A | G | 10 | a0001c0001t0010g0067 a0001c0001t0010g0093 a0001c0001t0010g0098 others(7): Show |
10 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1225+810A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887361 | |||||||
| chr3:189887424 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1225+873C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887424 | |||||||
| chr3:189887430 | A | G | 1 | a0001c0001t0017g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1225+879A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887430 | |||||||
| chr3:189887491 | G | T | 2 | a0001c0001t0018g0070 a0001c0001t0029g0048 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1225+940G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887491 | |||||||
| chr3:189887501 | A | G | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225+950A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887501 | |||||||
| chr3:189887518 | G | T | 5 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0018g0070 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+967G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887518 | |||||||
| chr3:189887621 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG04204.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1225+1070G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887621 | |||||||
| chr3:189887768 | G | T | 1 | a0001c0001t0003g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1225+1217G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887768 | |||||||
| chr3:189887856 | G | GT | 247 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0062 others(244): Show |
248 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1225+1323dupT | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 189887856 | ||||||
| chr3:189887856 | G | GTT | 18 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0168 others(15): Show |
18 | HG01175.hp2 HG01255.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1225+1322_1225+132 others(6): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 189887856 | ||||||
| chr3:189887861 | T | TG | 87 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0108 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1225+1310_1225+131 others(5): Show |
TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887861 | |||||||
| chr3:189887862 | T | G | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1225+1311T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887862 | |||||||
| chr3:189887886 | C | T | 1 | a0001c0001t0019g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1225+1335C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887886 | |||||||
| chr3:189887887 | G | A | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+1336G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887887 | |||||||
| chr3:189887969 | G | T | 15 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0001g0126 others(12): Show |
15 | HG00558.hp1 HG00673.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1226-1371G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887969 | |||||||
| chr3:189887982 | G | A | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-1358G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887982 | |||||||
| chr3:189887987 | G | C | 1 | a0001c0001t0001g0356 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1226-1353G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189887987 | |||||||
| chr3:189888003 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0134 |
2 | HG02129.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1226-1337T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888003 | |||||||
| chr3:189888017 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1226-1323C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888017 | |||||||
| chr3:189888058 | A | C | 1 | a0001c0001t0033g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1226-1282A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888058 | |||||||
| chr3:189888179 | A | T | 1 | a0001c0002t0009g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1226-1161A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888179 | |||||||
| chr3:189888217 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1226-1123C>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888217 | |||||||
| chr3:189888242 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0363 a0001c0001t0001g0365 others(1): Show |
4 | NA18975.hp1 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-1098A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888242 | |||||||
| chr3:189888537 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1226-803G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888537 | |||||||
| chr3:189888538 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1226-802G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888538 | |||||||
| chr3:189888682 | G | A | 5 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0018g0070 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-658G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888682 | |||||||
| chr3:189888761 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1226-579T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189888761 | |||||||
| chr3:189889090 | A | G | 1 | a0001c0001t0016g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1226-250A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189889090 | |||||||
| chr3:189889214 | C | T | 2 | a0001c0001t0025g0025 a0001c0001t0025g0041 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1226-126C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189889214 | |||||||
| chr3:189889311 | C | A | 4 | a0001c0001t0002g0026 a0001c0001t0011g0382 a0001c0001t0017g0160 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-29C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 9/11 | chr3 | 189889311 | |||||||
| chr3:189889530 | G | A | 4 | a0001c0001t0020g0284 a0001c0001t0020g0330 a0001c0001t0024g0015 others(1): Show |
4 | HG01978.hp1 HG02015.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370+46G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189889530 | |||||||
| chr3:189889603 | G | A | 1 | a0001c0001t0003g0353 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1370+119G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189889603 | |||||||
| chr3:189889784 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1370+300G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189889784 | |||||||
| chr3:189889825 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0039 |
3 | HG02055.hp1 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1370+341A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189889825 | |||||||
| chr3:189889837 | A | G | 158 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(155): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1370+353A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189889837 | |||||||
| chr3:189890187 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1371-602G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189890187 | |||||||
| chr3:189890278 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0251 |
2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1371-511C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189890278 | |||||||
| chr3:189890525 | C | T | 7 | a0001c0001t0011g0386 a0001c0001t0011g0390 a0001c0001t0011g0391 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1371-264C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189890525 | |||||||
| chr3:189890653 | T | G | 1 | a0001c0001t0002g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1371-136T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 10/11 | chr3 | 189890653 | |||||||
| chr3:189890945 | G | A | 1 | a0001c0001t0017g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1464+63G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189890945 | |||||||
| chr3:189891023 | A | G | 7 | a0001c0001t0039g0232 a0001c0002t0009g0084 a0001c0002t0009g0085 others(4): Show |
7 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+141A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891023 | |||||||
| chr3:189891172 | C | A | 267 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(264): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1464+290C>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891172 | |||||||
| chr3:189891173 | A | T | 2 | a0001c0001t0019g0174 a0001c0001t0019g0297 |
2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1464+291A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891173 | |||||||
| chr3:189891174 | T | A | 2 | a0001c0001t0033g0291 a0001c0001t0038g0033 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1464+292T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891174 | |||||||
| chr3:189891311 | G | C | 79 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(76): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1464+429G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891311 | |||||||
| chr3:189891481 | T | C | 5 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0018g0070 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+599T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891481 | |||||||
| chr3:189891613 | G | T | 71 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0080 others(68): Show |
71 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1464+731G>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891613 | |||||||
| chr3:189891678 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0002g0071 a0001c0001t0002g0073 |
3 | HG02970.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1464+796G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891678 | |||||||
| chr3:189891707 | T | C | 1 | a0001c0001t0011g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1464+825T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891707 | |||||||
| chr3:189891777 | G | A | 1 | a0001c0001t0008g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1464+895G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891777 | |||||||
| chr3:189891842 | G | A | 1 | a0001c0001t0014g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1464+960G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891842 | |||||||
| chr3:189891859 | A | G | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0038 |
3 | HG01074.hp1 HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1464+977A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891859 | |||||||
| chr3:189891901 | T | C | 5 | a0001c0001t0018g0031 a0001c0001t0018g0036 a0001c0001t0018g0070 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+1019T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189891901 | |||||||
| chr3:189892126 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0366 a0001c0001t0002g0127 |
3 | HG00408.hp2 HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1464+1244G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892126 | |||||||
| chr3:189892559 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1465-1647G>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892559 | |||||||
| chr3:189892628 | T | C | 8 | a0001c0001t0015g0146 a0001c0001t0015g0147 a0001c0001t0015g0148 others(5): Show |
8 | HG00642.hp2 HG01106.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-1578T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892628 | |||||||
| chr3:189892643 | T | G | 27 | a0001c0001t0002g0275 a0001c0001t0002g0300 a0001c0001t0005g0089 others(24): Show |
27 | HG01243.hp2 HG01255.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.1465-1563T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892643 | |||||||
| chr3:189892809 | G | A | 3 | a0001c0001t0003g0037 a0001c0001t0004g0074 a0001c0001t0004g0077 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1465-1397G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892809 | |||||||
| chr3:189892927 | C | T | 1 | a0001c0001t0001g0366 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1465-1279C>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189892927 | |||||||
| chr3:189893035 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1465-1171A>T | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893035 | |||||||
| chr3:189893112 | T | A | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0038 |
3 | HG01074.hp1 HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1465-1094T>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893112 | |||||||
| chr3:189893237 | A | G | 85 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1465-969A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893237 | |||||||
| chr3:189893254 | A | G | 1 | a0001c0001t0005g0158 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1465-952A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893254 | |||||||
| chr3:189893348 | A | G | 6 | a0001c0002t0009g0084 a0001c0002t0009g0085 a0001c0002t0009g0086 others(3): Show |
6 | HG02135.hp1 HG02523.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-858A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893348 | |||||||
| chr3:189893390 | G | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0298 others(3): Show |
6 | HG00639.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-816G>A | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893390 | |||||||
| chr3:189893405 | T | C | 145 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(142): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1465-801T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893405 | |||||||
| chr3:189893483 | A | C | 1 | a0001c0001t0002g0257 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1465-723A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893483 | |||||||
| chr3:189893498 | A | G | 7 | a0001c0001t0001g0299 a0001c0001t0001g0384 a0001c0001t0002g0292 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-708A>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893498 | |||||||
| chr3:189893733 | T | G | 4 | a0001c0001t0003g0318 a0001c0001t0003g0341 a0001c0001t0016g0316 others(1): Show |
4 | HG04115.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-473T>G | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893733 | |||||||
| chr3:189893765 | A | C | 1 | a0001c0001t0003g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1465-441A>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893765 | |||||||
| chr3:189893916 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1465-290T>C | TP63 | ENSG00000073282.14 | transcript | ENST00000354600.10 | protein_coding | 11/11 | chr3 | 189893916 |