Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83741 |
| ensemblid | ENSG00000008197.5 |
| hgncid | 15581 |
| symbol | TFAP2D |
| name | transcription factor AP-2 delta |
| refseq_nuc | NM_172238.4 |
| refseq_prot | NP_758438.2 |
| ensembl_nuc | ENST00000008391.4 |
| ensembl_prot | ENSP00000008391.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 50713526 |
| end | 50773033 |
| strand | + |
| ver | v1.2 |
| region | chr6:50713526-50773033 |
| region5000 | chr6:50708526-50778033 |
| regionname0 | TFAP2D_chr6_50713526_50773033 |
| regionname5000 | TFAP2D_chr6_50708526_50778033 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 302 | 90 | 61 | 101 | 12 | 36 | 75 | TFAP2D_chr6_50708526_50778033 | TFAP2D | MSTTF others(447): Show |
chr6 | 50708526 | 50778033 |
| a0002 | 0/0 | 452 | 31 | 0 | 2 | 25 | 2 | 2 | 19 | TFAP2D_chr6_50708526_50778033 | TFAP2D | MSTTF others(447): Show |
chr6 | 50708526 | 50778033 |
| a0003 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | MSTTF others(447): Show |
chr6 | 50708526 | 50778033 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 295 | 84 | 61 | 100 | 12 | 36 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 | ||
| a0001c0003 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 | ||
| a0001c0005 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 | ||
| a0001c0006 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 | ||
| a0002c0002 | 0/0 | 1356 | 31 | 0 | 2 | 25 | 2 | 2 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 | ||
| a0003c0004 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | ATGTC others(1351): Show |
chr6 | 50708526 | 50778033 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2058 | 152 | 44 | 39 | 38 | 7 | 23 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0002 | 0/1 | 2058 | 73 | 4 | 13 | 46 | 2 | 7 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0003 | 0/0 | 2057 | 55 | 36 | 2 | 14 | 0 | 3 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2052): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0004 | 0/0 | 2059 | 12 | 0 | 6 | 1 | 3 | 2 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2054): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0005 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0006 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0001t0007 | 0/0 | 2058 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0003t0001 | 0/0 | 2058 | 5 | 5 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0005t0001 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0001c0006t0002 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0002c0002t0001 | 0/0 | 2058 | 29 | 0 | 2 | 24 | 1 | 2 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| a0002c0002t0003 | 0/0 | 2057 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2052): Show |
chr6 | 50708526 | 50778033 |
| a0002c0002t0004 | 0/0 | 2059 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2054): Show |
chr6 | 50708526 | 50778033 |
| a0003c0004t0002 | 0/0 | 2058 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | AGCTA others(2053): Show |
chr6 | 50708526 | 50778033 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0001 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0001c0006t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0002c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| a0003c0004t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0297 | EUR | GBR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00673 | hp2 | a0002 | c0002 | t0004 | g0279 | EAS | CHS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0109 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01192 | hp1 | a0003 | c0004 | t0002 | g0247 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0084 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0086 | EUR | IBS | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CDX | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | CDX | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CDX | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0301 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0278 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0290 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0298 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0088 | SAS | PJL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | STU | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | YRI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18953 | hp2 | a0001 | c0006 | t0002 | g0056 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0038 | EUR | TSI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0085 | EUR | TSI | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | USA | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | USA | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0114 | REF | REF | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0191 | REF | REF | TFAP2D_chr6_50708526_50778033 | TFAP2D | chr6 | 50708526 | 50778033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50715296 | T | C | 1 | a0002 | 31 | HG00140.hp2 HG00621.hp1 HG00673.hp2 others(28): Show |
missense_variant | MODERATE | c.220T>C | p.Phe74Leu | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/8 | 750/2058 | 220/1359 | 74/452 | chr6 | 50715296 | |||
| chr6:50772775 | G | A | 1 | a0003 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.1270G>A | p.Gly424Ser | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 8/8 | 1800/2058 | 1270/1359 | 424/452 | chr6 | 50772775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50715298 | C | T | 1 | a0001c0006 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.222C>T | p.Phe74Phe | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/8 | 752/2058 | 222/1359 | 74/452 | chr6 | 50715298 | |||
| chr6:50715481 | C | T | 1 | a0001c0005 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.405C>T | p.Gly135Gly | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/8 | 935/2058 | 405/1359 | 135/452 | chr6 | 50715481 | |||
| chr6:50745225 | A | G | 1 | a0001c0003 | 5 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
synonymous_variant | LOW | c.1002A>G | p.Arg334Arg | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/8 | 1532/2058 | 1002/1359 | 334/452 | chr6 | 50745225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50713714 | T | C | 1 | a0001c0001t0005 | 1 | NA19054.hp2 | 5_prime_UTR_variant | MODIFIER | c.-342T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/8 | 342 | chr6 | 50713714 | ||||||
| chr6:50713947 | AT | A | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0006t0002 others(2): Show |
130 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(127): Show |
5_prime_UTR_variant | MODIFIER | c.-99delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/8 | 99 | INFO_REALIGN_3_PRIME | chr6 | 50713947 | |||||
| chr6:50713978 | C | G | 1 | a0001c0001t0007 | 1 | HG00738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/8 | 78 | chr6 | 50713978 | ||||||
| chr6:50773018 | A | G | 1 | a0001c0001t0006 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*154A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 8/8 | 154 | chr6 | 50773018 | ||||||
| chr6:50773032 | C | CA | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0006t0002 others(2): Show |
87 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*158dupA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 8/8 | 159 | INFO_REALIGN_3_PRIME | chr6 | 50773032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50714104 | C | CT | 95 | a0001c0001t0001g0288 a0001c0001t0001g0303 a0001c0001t0001g0304 others(92): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.39+30dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 50714104 | ||||||
| chr6:50714104 | C | CTT | 9 | a0001c0001t0001g0315 a0001c0001t0002g0307 a0001c0001t0002g0309 others(6): Show |
9 | HG00597.hp2 HG02523.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+29_39+30dupTT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 50714104 | ||||||
| chr6:50714104 | CT | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0058 others(72): Show |
77 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.39+30delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 50714104 | ||||||
| chr6:50714104 | CTT | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00741.hp2 HG01069.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+29_39+30delTT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 50714104 | ||||||
| chr6:50714598 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0110 a0001c0001t0007g0109 |
3 | HG00738.hp2 HG02683.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.39+504T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714598 | |||||||
| chr6:50714676 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.40-440T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714676 | |||||||
| chr6:50714763 | G | A | 31 | a0001c0001t0002g0053 a0001c0001t0002g0055 a0001c0001t0003g0004 others(28): Show |
32 | HG01123.hp2 HG01891.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.40-353G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714763 | |||||||
| chr6:50714803 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.40-296_40-283delTG others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 50714803 | ||||||
| chr6:50714892 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.40-224G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714892 | |||||||
| chr6:50714900 | G | A | 1 | a0002c0002t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.40-216G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714900 | |||||||
| chr6:50714903 | T | A | 1 | a0001c0001t0003g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.40-213T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714903 | |||||||
| chr6:50714997 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.40-119C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50714997 | |||||||
| chr6:50715052 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0004g0218 |
2 | HG00642.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.40-64C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 1/7 | chr6 | 50715052 | |||||||
| chr6:50715658 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.537+45C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715658 | |||||||
| chr6:50715702 | CTCTT | C | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.537+93_537+96delTT others(2): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715702 | ||||||
| chr6:50715721 | CCT | C | 40 | a0001c0001t0001g0079 a0001c0001t0001g0115 a0001c0001t0001g0136 others(37): Show |
40 | HG00597.hp2 HG00621.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.537+136_537+137del others(2): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715721 | ||||||
| chr6:50715721 | CCTCT | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
175 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.537+134_537+137del others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715721 | ||||||
| chr6:50715721 | CCTCTCT | C | 3 | a0001c0001t0003g0042 a0001c0001t0003g0047 a0001c0001t0003g0054 |
3 | HG01123.hp2 HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.537+132_537+137del others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715721 | ||||||
| chr6:50715721 | CCTCTCTC others(1): Show |
C | 5 | a0001c0001t0002g0003 a0002c0002t0001g0291 a0002c0002t0001g0292 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.537+130_537+137del others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715721 | ||||||
| chr6:50715737 | TCTCTCTC others(7): Show |
T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.537+126_537+139del others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715737 | ||||||
| chr6:50715743 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0002g0238 |
2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.537+130T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715743 | |||||||
| chr6:50715743 | T | TCACA | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0003t0001g0301 |
3 | HG02615.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.537+131_537+132ins others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715743 | ||||||
| chr6:50715745 | T | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0146 a0001c0001t0001g0214 others(12): Show |
15 | HG00738.hp1 HG01433.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.537+132T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715745 | |||||||
| chr6:50715745 | T | TCACA | 4 | a0001c0003t0001g0081 a0001c0003t0001g0098 a0001c0003t0001g0102 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+133_537+134ins others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715745 | ||||||
| chr6:50715745 | TCTCTCA | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01069.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+134_537+139del others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715745 | ||||||
| chr6:50715745 | TCTCTCAC others(7): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.537+134_537+147del others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715745 | ||||||
| chr6:50715747 | T | A | 71 | a0001c0001t0001g0079 a0001c0001t0001g0135 a0001c0001t0001g0136 others(68): Show |
72 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.537+134T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715747 | |||||||
| chr6:50715747 | T | TCA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0089 others(3): Show |
7 | HG01169.hp1 HG02683.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.537+135_537+136ins others(2): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715747 | ||||||
| chr6:50715749 | T | A | 279 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.537+136T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715749 | |||||||
| chr6:50715749 | T | TCA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0093 a0001c0001t0001g0168 others(1): Show |
4 | HG01346.hp1 HG02630.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+166_537+167dup others(2): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50715749 | ||||||
| chr6:50715906 | G | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0115 others(8): Show |
13 | HG00280.hp2 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+293G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715906 | |||||||
| chr6:50715987 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG00544.hp2 HG00673.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+374G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50715987 | |||||||
| chr6:50716157 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.537+544A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716157 | |||||||
| chr6:50716161 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.537+548A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716161 | |||||||
| chr6:50716459 | A | AAAGG | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(106): Show |
120 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.537+859_537+862dup others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50716459 | ||||||
| chr6:50716476 | G | A | 1 | a0001c0001t0003g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.537+863G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716476 | |||||||
| chr6:50716479 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.537+866A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716479 | |||||||
| chr6:50716481 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.537+868A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716481 | |||||||
| chr6:50716484 | G | A | 1 | a0001c0001t0003g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.537+871G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716484 | |||||||
| chr6:50716592 | C | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.537+979C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716592 | |||||||
| chr6:50716684 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.537+1071C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716684 | |||||||
| chr6:50716899 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.537+1286G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716899 | |||||||
| chr6:50716909 | T | C | 3 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 |
3 | HG02145.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.537+1296T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50716909 | |||||||
| chr6:50717017 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0307 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.537+1404G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717017 | |||||||
| chr6:50717066 | G | C | 3 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | NA18968.hp2 NA18974.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.537+1453G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717066 | |||||||
| chr6:50717120 | T | C | 1 | a0002c0002t0003g0038 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.537+1507T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717120 | |||||||
| chr6:50717130 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.537+1517C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717130 | |||||||
| chr6:50717841 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538-1249G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717841 | |||||||
| chr6:50717882 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538-1208A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50717882 | |||||||
| chr6:50718029 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.538-1061C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50718029 | |||||||
| chr6:50718120 | G | GT | 45 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(42): Show |
45 | HG01069.hp2 HG01123.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.538-958dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 50718120 | ||||||
| chr6:50718128 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02071.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.538-962T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50718128 | |||||||
| chr6:50718314 | G | A | 1 | a0002c0002t0001g0274 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.538-776G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50718314 | |||||||
| chr6:50718715 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.538-375C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50718715 | |||||||
| chr6:50718771 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG00544.hp2 HG00673.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.538-319C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 2/7 | chr6 | 50718771 | |||||||
| chr6:50719222 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.598+72G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50719222 | |||||||
| chr6:50719447 | G | GAGAA | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
98 | HG00280.hp1 HG00673.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.598+350_598+353dup others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | G | GAGAAAGA others(1): Show |
43 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0070 others(40): Show |
44 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.598+346_598+353dup others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | G | GAGAAAGA others(5): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG02155.hp2 HG02293.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+342_598+353dup others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | G | GAGAAGAA others(4): Show |
2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02080.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.598+301_598+302ins others(11): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | GAGAA | G | 13 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0202 others(10): Show |
13 | HG00099.hp2 HG01123.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+350_598+353del others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | GAGAAAGA others(1): Show |
G | 9 | a0001c0001t0001g0123 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+346_598+353del others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | GAGAAAGA others(5): Show |
G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0207 a0001c0001t0001g0208 others(4): Show |
8 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+342_598+353del others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719447 | GAGAAAGA others(21): Show |
G | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.598+326_598+353del others(28): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719447 | ||||||
| chr6:50719473 | G | T | 1 | a0001c0001t0003g0269 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.598+323G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50719473 | |||||||
| chr6:50719478 | A | AAAGAAAG others(13): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.598+347_598+348ins others(20): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719478 | ||||||
| chr6:50719478 | A | AAAGAAAG others(9): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.598+343_598+344ins others(16): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719478 | ||||||
| chr6:50719478 | A | AAAGAAAG others(5): Show |
1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+339_598+340ins others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719478 | ||||||
| chr6:50719498 | AAAG | A | 22 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0002 others(19): Show |
22 | HG00408.hp1 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.598+352_598+354del others(3): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719498 | ||||||
| chr6:50719501 | G | GA | 21 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(18): Show |
25 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.598+353dupA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719501 | ||||||
| chr6:50719501 | G | GAAAGA | 14 | a0001c0001t0002g0014 a0001c0001t0002g0126 a0001c0001t0002g0127 others(11): Show |
14 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.598+353_598+354ins others(5): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719501 | ||||||
| chr6:50719501 | G | GAAAGAAA others(2): Show |
9 | a0001c0001t0002g0053 a0001c0001t0002g0128 a0001c0001t0002g0231 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+353_598+354ins others(9): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719501 | ||||||
| chr6:50719501 | G | GAAAGAAA others(6): Show |
3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0002g0264 |
3 | HG00738.hp1 HG01109.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.598+353_598+354ins others(13): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719501 | ||||||
| chr6:50719501 | G | GAAAGAAA others(14): Show |
1 | a0001c0001t0002g0003 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.598+353_598+354ins others(21): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719501 | ||||||
| chr6:50719502 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0142 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.598+353_598+354ins others(11): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50719502 | ||||||
| chr6:50719633 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+483G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50719633 | |||||||
| chr6:50720222 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0112 |
3 | HG02486.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.598+1072C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720222 | |||||||
| chr6:50720385 | T | G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.598+1235T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720385 | |||||||
| chr6:50720414 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.598+1264G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720414 | |||||||
| chr6:50720470 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598+1320A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720470 | |||||||
| chr6:50720485 | AAACACAC others(8): Show |
A | 2 | a0001c0001t0002g0268 a0001c0001t0003g0308 |
2 | NA18971.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.598+1337_598+1351d others(17): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720485 | ||||||
| chr6:50720486 | A | AAC | 20 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0036 others(17): Show |
22 | HG00408.hp2 HG01346.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.598+1388_598+1389d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | A | AACAC | 9 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0166 others(6): Show |
10 | HG00738.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+1386_598+1389d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | A | AACACAC | 4 | a0001c0001t0003g0054 a0001c0001t0003g0057 a0001c0001t0003g0113 others(1): Show |
4 | HG01123.hp2 HG02647.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+1384_598+1389d others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.598+1336A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720486 | |||||||
| chr6:50720486 | AAC | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
44 | HG00280.hp2 HG00642.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.598+1388_598+1389d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACAC | A | 39 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0080 others(36): Show |
39 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.598+1386_598+1389d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACAC | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0023 others(49): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.598+1384_598+1389d others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(1): Show |
A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0074 a0001c0001t0001g0091 others(9): Show |
12 | HG01074.hp2 HG02155.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+1382_598+1389d others(10): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(3): Show |
A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0004g0085 |
3 | HG00639.hp1 NA19081.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.598+1380_598+1389d others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(5): Show |
A | 4 | a0001c0001t0001g0108 a0001c0001t0002g0258 a0001c0001t0003g0124 others(1): Show |
4 | HG01433.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+1378_598+1389d others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(7): Show |
A | 15 | a0001c0001t0002g0134 a0001c0001t0002g0222 a0001c0001t0002g0235 others(12): Show |
15 | HG02074.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.598+1376_598+1389d others(16): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(9): Show |
A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(53): Show |
62 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.598+1374_598+1389d others(18): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(11): Show |
A | 7 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+1372_598+1389d others(20): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720486 | AACACACA others(13): Show |
A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG00544.hp2 HG00673.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+1370_598+1389d others(22): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720486 | ||||||
| chr6:50720519 | A | T | 3 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 |
3 | HG02145.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.598+1369A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720519 | |||||||
| chr6:50720522 | CACACACA others(11): Show |
C | 1 | a0001c0001t0002g0267 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.598+1374_598+1391d others(20): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50720522 | ||||||
| chr6:50720540 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.598+1390T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720540 | |||||||
| chr6:50720737 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
6 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+1587T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720737 | |||||||
| chr6:50720751 | A | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0186 a0001c0001t0001g0201 others(1): Show |
4 | HG00639.hp1 HG01934.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+1601A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720751 | |||||||
| chr6:50720842 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.598+1692C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50720842 | |||||||
| chr6:50721047 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.598+1897C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721047 | |||||||
| chr6:50721053 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.598+1903T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721053 | |||||||
| chr6:50721083 | G | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0001g0152 others(5): Show |
8 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+1933G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721083 | |||||||
| chr6:50721120 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.598+1970G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721120 | |||||||
| chr6:50721155 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0103 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.598+2005T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721155 | |||||||
| chr6:50721185 | A | G | 5 | a0001c0003t0001g0081 a0001c0003t0001g0098 a0001c0003t0001g0102 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+2035A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721185 | |||||||
| chr6:50721439 | C | A | 1 | a0002c0002t0001g0285 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.598+2289C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721439 | |||||||
| chr6:50721468 | G | A | 22 | a0001c0001t0002g0055 a0001c0001t0003g0004 a0001c0001t0003g0037 others(19): Show |
23 | HG01123.hp2 HG01891.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.598+2318G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721468 | |||||||
| chr6:50721602 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.598+2452A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721602 | |||||||
| chr6:50721879 | A | C | 1 | a0001c0001t0003g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.598+2729A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721879 | |||||||
| chr6:50721899 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.598+2749T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721899 | |||||||
| chr6:50721930 | A | G | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.598+2780A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50721930 | |||||||
| chr6:50722246 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+3096A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722246 | |||||||
| chr6:50722385 | T | A | 1 | a0001c0001t0002g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.598+3235T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722385 | |||||||
| chr6:50722469 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0039 |
4 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+3319G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722469 | |||||||
| chr6:50722571 | C | G | 1 | a0001c0001t0003g0113 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598+3421C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722571 | |||||||
| chr6:50722717 | A | C | 1 | a0001c0001t0003g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598+3567A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722717 | |||||||
| chr6:50722774 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.598+3624G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722774 | |||||||
| chr6:50722813 | A | AG | 55 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0094 others(52): Show |
55 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.598+3671dupG | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50722813 | ||||||
| chr6:50722844 | T | C | 1 | a0001c0001t0002g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.598+3694T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722844 | |||||||
| chr6:50722886 | A | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0182 |
2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.598+3736A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722886 | |||||||
| chr6:50722898 | T | A | 1 | a0001c0005t0001g0278 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+3748T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722898 | |||||||
| chr6:50722975 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.598+3825A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722975 | |||||||
| chr6:50722977 | G | C | 1 | a0001c0001t0004g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.598+3827G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50722977 | |||||||
| chr6:50723139 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+3989G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50723139 | |||||||
| chr6:50723657 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+4507A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50723657 | |||||||
| chr6:50723839 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.598+4689A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50723839 | |||||||
| chr6:50724095 | G | C | 3 | a0002c0002t0001g0286 a0002c0002t0001g0300 a0002c0002t0001g0302 |
3 | HG02135.hp2 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.599-4761G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724095 | |||||||
| chr6:50724118 | A | AG | 14 | a0001c0001t0001g0073 a0001c0001t0001g0305 a0001c0001t0004g0027 others(11): Show |
14 | HG01071.hp2 HG01255.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.599-4734dupG | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50724118 | ||||||
| chr6:50724226 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.599-4630C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724226 | |||||||
| chr6:50724265 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.599-4591A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724265 | |||||||
| chr6:50724381 | T | C | 12 | a0001c0001t0002g0055 a0001c0001t0003g0004 a0001c0001t0003g0037 others(9): Show |
13 | HG01891.hp2 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-4475T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724381 | |||||||
| chr6:50724460 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-4396C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724460 | |||||||
| chr6:50724490 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0100 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.599-4366G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724490 | |||||||
| chr6:50724527 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.599-4329G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724527 | |||||||
| chr6:50724545 | G | T | 1 | a0001c0001t0002g0309 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.599-4311G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724545 | |||||||
| chr6:50724579 | G | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-4277G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724579 | |||||||
| chr6:50724638 | C | G | 75 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0002g0001 others(72): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.599-4218C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724638 | |||||||
| chr6:50724737 | TC | T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.599-4117delC | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50724737 | ||||||
| chr6:50724847 | A | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0154 others(20): Show |
24 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.599-4009A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724847 | |||||||
| chr6:50724892 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.599-3964C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50724892 | |||||||
| chr6:50724976 | GGACA | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-3876_599-3873d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 50724976 | ||||||
| chr6:50725115 | C | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.599-3741C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50725115 | |||||||
| chr6:50725194 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-3662A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50725194 | |||||||
| chr6:50725793 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.599-3063T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50725793 | |||||||
| chr6:50725894 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(142): Show |
157 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.599-2962T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50725894 | |||||||
| chr6:50726143 | C | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.599-2713C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726143 | |||||||
| chr6:50726145 | T | G | 1 | a0001c0001t0003g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.599-2711T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726145 | |||||||
| chr6:50726146 | G | T | 1 | a0001c0001t0003g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.599-2710G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726146 | |||||||
| chr6:50726339 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.599-2517G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726339 | |||||||
| chr6:50726361 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.599-2495T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726361 | |||||||
| chr6:50726747 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599-2109T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726747 | |||||||
| chr6:50726984 | T | C | 81 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(78): Show |
91 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.599-1872T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726984 | |||||||
| chr6:50726989 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599-1867G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50726989 | |||||||
| chr6:50727275 | A | G | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(71): Show |
84 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.599-1581A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50727275 | |||||||
| chr6:50727643 | T | C | 119 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
130 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.599-1213T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50727643 | |||||||
| chr6:50727789 | T | C | 119 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
130 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.599-1067T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50727789 | |||||||
| chr6:50727807 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.599-1049A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50727807 | |||||||
| chr6:50727965 | T | C | 1 | a0001c0003t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.599-891T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50727965 | |||||||
| chr6:50728014 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0115 others(8): Show |
13 | HG00280.hp2 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-842G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728014 | |||||||
| chr6:50728103 | A | G | 2 | a0001c0001t0003g0249 a0001c0001t0003g0250 |
2 | NA18961.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.599-753A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728103 | |||||||
| chr6:50728484 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.599-372C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728484 | |||||||
| chr6:50728715 | C | A | 1 | a0002c0002t0001g0294 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.599-141C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728715 | |||||||
| chr6:50728718 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0112 |
3 | HG02486.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.599-138C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728718 | |||||||
| chr6:50728733 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.599-123T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 3/7 | chr6 | 50728733 | |||||||
| chr6:50729606 | C | A | 10 | a0001c0001t0004g0027 a0001c0001t0004g0071 a0001c0001t0004g0072 others(7): Show |
10 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.883+294C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50729606 | |||||||
| chr6:50729689 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
7 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.883+377A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50729689 | |||||||
| chr6:50729751 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.883+439G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50729751 | |||||||
| chr6:50729769 | A | G | 1 | a0001c0001t0002g0265 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883+457A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50729769 | |||||||
| chr6:50730095 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.883+783G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730095 | |||||||
| chr6:50730178 | G | A | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.883+866G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730178 | |||||||
| chr6:50730512 | GA | G | 16 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(13): Show |
16 | HG01123.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.883+1209delA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50730512 | ||||||
| chr6:50730529 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.883+1217T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730529 | |||||||
| chr6:50730735 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+1423C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730735 | |||||||
| chr6:50730748 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.883+1436C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730748 | |||||||
| chr6:50730824 | G | A | 2 | a0001c0001t0003g0004 a0001c0001t0003g0039 |
3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.883+1512G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50730824 | |||||||
| chr6:50731043 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0103 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.883+1731C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731043 | |||||||
| chr6:50731187 | G | T | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.883+1875G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731187 | |||||||
| chr6:50731412 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.883+2100C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731412 | |||||||
| chr6:50731449 | T | TAC | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
25 | HG00733.hp2 HG00741.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.883+2161_883+2162d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50731449 | ||||||
| chr6:50731449 | TAC | T | 105 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(102): Show |
114 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.883+2161_883+2162d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50731449 | ||||||
| chr6:50731476 | T | A | 1 | a0001c0006t0002g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.883+2164T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731476 | |||||||
| chr6:50731579 | T | G | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.883+2267T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731579 | |||||||
| chr6:50731636 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
7 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.883+2324G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731636 | |||||||
| chr6:50731978 | A | C | 2 | a0001c0001t0001g0030 a0001c0001t0003g0101 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.883+2666A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50731978 | |||||||
| chr6:50732063 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.883+2751G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732063 | |||||||
| chr6:50732157 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.883+2845A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732157 | |||||||
| chr6:50732227 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.883+2915G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732227 | |||||||
| chr6:50732642 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883+3330A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732642 | |||||||
| chr6:50732761 | A | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(99): Show |
112 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.883+3449A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732761 | |||||||
| chr6:50732858 | A | T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.883+3546A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50732858 | |||||||
| chr6:50733030 | C | G | 1 | a0001c0001t0003g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883+3718C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50733030 | |||||||
| chr6:50733794 | G | T | 1 | a0001c0001t0003g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.883+4482G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50733794 | |||||||
| chr6:50733839 | G | A | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+4527G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50733839 | |||||||
| chr6:50733874 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0211 |
2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.883+4562C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50733874 | |||||||
| chr6:50733888 | A | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+4576A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50733888 | |||||||
| chr6:50733986 | A | ATG | 32 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0136 others(29): Show |
32 | HG00673.hp2 HG01261.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.883+4706_883+4707d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50733986 | ||||||
| chr6:50733986 | A | ATGTG | 15 | a0001c0001t0001g0135 a0001c0001t0001g0155 a0001c0001t0001g0187 others(12): Show |
15 | HG00597.hp1 HG01123.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.883+4704_883+4707d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50733986 | ||||||
| chr6:50733986 | ATG | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0065 others(13): Show |
17 | HG00544.hp2 HG02004.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+4706_883+4707d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50733986 | ||||||
| chr6:50733986 | ATGTGTG | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+4702_883+4707d others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50733986 | ||||||
| chr6:50734387 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.883+5075G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734387 | |||||||
| chr6:50734557 | T | C | 4 | a0001c0003t0001g0081 a0001c0003t0001g0098 a0001c0003t0001g0102 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+5245T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734557 | |||||||
| chr6:50734771 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01074.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.883+5459C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734771 | |||||||
| chr6:50734772 | G | A | 43 | a0001c0001t0001g0028 a0001c0001t0001g0073 a0001c0001t0001g0074 others(40): Show |
44 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.883+5460G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734772 | |||||||
| chr6:50734804 | A | C | 2 | a0002c0002t0001g0291 a0002c0002t0001g0292 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.883+5492A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734804 | |||||||
| chr6:50734908 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.883+5596C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734908 | |||||||
| chr6:50734936 | T | C | 12 | a0001c0001t0002g0055 a0001c0001t0003g0004 a0001c0001t0003g0037 others(9): Show |
13 | HG01891.hp2 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.883+5624T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50734936 | |||||||
| chr6:50735121 | A | G | 27 | a0001c0001t0002g0055 a0001c0001t0003g0004 a0001c0001t0003g0037 others(24): Show |
28 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.883+5809A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735121 | |||||||
| chr6:50735361 | G | A | 145 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(142): Show |
156 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.883+6049G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735361 | |||||||
| chr6:50735402 | C | T | 13 | a0001c0001t0001g0096 a0001c0001t0001g0147 a0001c0001t0001g0148 others(10): Show |
13 | HG00735.hp1 HG00741.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.883+6090C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735402 | |||||||
| chr6:50735612 | G | A | 104 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(101): Show |
114 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.883+6300G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735612 | |||||||
| chr6:50735707 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0003g0101 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.883+6395T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735707 | |||||||
| chr6:50735781 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0233 a0001c0001t0002g0234 others(1): Show |
5 | HG00408.hp1 HG00438.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+6469G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50735781 | |||||||
| chr6:50736124 | C | T | 1 | a0001c0003t0001g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883+6812C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736124 | |||||||
| chr6:50736167 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0003g0101 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.883+6855G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736167 | |||||||
| chr6:50736172 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+6860G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736172 | |||||||
| chr6:50736355 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.883+7043G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736355 | |||||||
| chr6:50736364 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.883+7052C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736364 | |||||||
| chr6:50736366 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.883+7054A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736366 | |||||||
| chr6:50736431 | C | G | 1 | a0001c0001t0002g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.883+7119C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736431 | |||||||
| chr6:50736473 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.883+7161A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736473 | |||||||
| chr6:50736485 | CTT | C | 4 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0282 others(1): Show |
4 | HG02155.hp2 NA18942.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+7174_883+7175d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736485 | |||||||
| chr6:50736515 | T | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(93): Show |
106 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.883+7203T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736515 | |||||||
| chr6:50736644 | T | A | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.883+7332T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736644 | |||||||
| chr6:50736775 | T | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+7463T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736775 | |||||||
| chr6:50736980 | G | T | 1 | a0002c0002t0001g0281 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.883+7668G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736980 | |||||||
| chr6:50736981 | T | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.883+7669T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50736981 | |||||||
| chr6:50737024 | A | G | 1 | a0002c0002t0001g0281 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.883+7712A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737024 | |||||||
| chr6:50737128 | A | G | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(305): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.883+7816A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737128 | |||||||
| chr6:50737218 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.884-7889C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737218 | |||||||
| chr6:50737335 | T | A | 102 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(99): Show |
112 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-7772T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737335 | |||||||
| chr6:50737379 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0183 |
2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.884-7728G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737379 | |||||||
| chr6:50737385 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.884-7722T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737385 | |||||||
| chr6:50737466 | T | C | 5 | a0001c0001t0001g0120 a0002c0002t0001g0291 a0002c0002t0001g0292 others(2): Show |
5 | HG00140.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-7641T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737466 | |||||||
| chr6:50737758 | G | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(23): Show |
27 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.884-7349G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737758 | |||||||
| chr6:50737761 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.884-7346G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737761 | |||||||
| chr6:50737882 | T | C | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-7225T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737882 | |||||||
| chr6:50737939 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.884-7168G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50737939 | |||||||
| chr6:50738331 | TG | T | 9 | a0001c0001t0004g0027 a0001c0001t0004g0072 a0001c0001t0004g0083 others(6): Show |
9 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.884-6773delG | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50738331 | ||||||
| chr6:50738472 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-6635T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50738472 | |||||||
| chr6:50738705 | A | G | 7 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG01123.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-6402A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50738705 | |||||||
| chr6:50739259 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.884-5848C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739259 | |||||||
| chr6:50739374 | A | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0203 |
3 | HG00099.hp2 HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.884-5733A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739374 | |||||||
| chr6:50739436 | G | T | 8 | a0002c0002t0001g0216 a0002c0002t0001g0275 a0002c0002t0001g0281 others(5): Show |
8 | HG02074.hp2 NA18969.hp1 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.884-5671G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739436 | |||||||
| chr6:50739605 | C | A | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.884-5502C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739605 | |||||||
| chr6:50739947 | T | C | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-5160T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739947 | |||||||
| chr6:50739961 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.884-5146T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50739961 | |||||||
| chr6:50740393 | T | G | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.884-4714T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740393 | |||||||
| chr6:50740394 | T | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(25): Show |
29 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.884-4713T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740394 | |||||||
| chr6:50740423 | T | TTTTG | 9 | a0001c0001t0002g0225 a0001c0001t0002g0265 a0001c0001t0003g0051 others(6): Show |
9 | HG01433.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-4660_884-4657d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50740423 | ||||||
| chr6:50740465 | A | G | 3 | a0001c0001t0001g0028 a0002c0002t0001g0285 a0002c0002t0001g0289 |
3 | NA18954.hp1 NA18955.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.884-4642A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740465 | |||||||
| chr6:50740582 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.884-4525G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740582 | |||||||
| chr6:50740602 | A | AT | 102 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(99): Show |
112 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-4497dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50740602 | ||||||
| chr6:50740678 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-4429C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740678 | |||||||
| chr6:50740684 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.884-4423G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740684 | |||||||
| chr6:50740732 | C | T | 21 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(18): Show |
21 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.884-4375C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740732 | |||||||
| chr6:50740911 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.884-4196A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50740911 | |||||||
| chr6:50741000 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0002g0225 |
2 | HG02886.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.884-4107C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741000 | |||||||
| chr6:50741092 | TGTATTTA others(6): Show |
T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0057 a0001c0003t0001g0102 |
3 | HG02647.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.884-3983_884-3971d others(15): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50741092 | ||||||
| chr6:50741257 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.884-3850C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741257 | |||||||
| chr6:50741275 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.884-3832A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741275 | |||||||
| chr6:50741315 | G | C | 3 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | NA18968.hp2 NA18974.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.884-3792G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741315 | |||||||
| chr6:50741406 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.884-3701C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741406 | |||||||
| chr6:50741490 | A | G | 1 | a0003c0004t0002g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.884-3617A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741490 | |||||||
| chr6:50741574 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.884-3533G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741574 | |||||||
| chr6:50741699 | T | TA | 25 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0002g0055 others(22): Show |
25 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.884-3398dupA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50741699 | ||||||
| chr6:50741699 | TA | T | 9 | a0001c0001t0002g0225 a0001c0001t0004g0027 a0001c0001t0004g0072 others(6): Show |
9 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.884-3398delA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50741699 | ||||||
| chr6:50741712 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.884-3395T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741712 | |||||||
| chr6:50741994 | A | G | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.884-3113A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50741994 | |||||||
| chr6:50742478 | C | G | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.884-2629C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742478 | |||||||
| chr6:50742524 | T | TTGGA | 4 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
5 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-2563_884-2560d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742524 | ||||||
| chr6:50742573 | C | CATAG | 15 | a0001c0001t0001g0096 a0001c0001t0001g0157 a0001c0001t0001g0161 others(12): Show |
15 | HG00733.hp2 HG00735.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.884-2479_884-2476d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742573 | ||||||
| chr6:50742573 | CATAG | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.884-2479_884-2476d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742573 | ||||||
| chr6:50742573 | CATAGATA others(1): Show |
C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(87): Show |
96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.884-2483_884-2476d others(10): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742573 | ||||||
| chr6:50742573 | CATAGATA others(5): Show |
C | 18 | a0001c0001t0001g0058 a0001c0001t0001g0094 a0001c0001t0001g0095 others(15): Show |
18 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.884-2487_884-2476d others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742573 | ||||||
| chr6:50742573 | CATAGATA others(9): Show |
C | 2 | a0001c0001t0001g0141 a0001c0001t0003g0049 |
2 | HG01934.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.884-2491_884-2476d others(18): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742573 | ||||||
| chr6:50742578 | A | ATAGT | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-2526_884-2525i others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742578 | ||||||
| chr6:50742582 | A | T | 2 | a0001c0001t0003g0020 a0001c0001t0003g0021 |
2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.884-2525A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742582 | |||||||
| chr6:50742586 | A | T | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.884-2521A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742586 | |||||||
| chr6:50742623 | TAGATAGA others(5): Show |
T | 1 | a0001c0001t0002g0242 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.884-2483_884-2472d others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742623 | |||||||
| chr6:50742627 | TAGATGAT others(1): Show |
T | 3 | a0001c0001t0001g0082 a0001c0001t0003g0101 a0001c0001t0004g0072 |
3 | HG02055.hp2 HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.884-2479_884-2472d others(10): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742627 | |||||||
| chr6:50742931 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-2176G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742931 | |||||||
| chr6:50742954 | A | AAC | 31 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0035 others(28): Show |
32 | HG00140.hp2 HG00597.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.884-2113_884-2112d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACAC | 25 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0076 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.884-2115_884-2112d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACAC | 6 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0194 others(3): Show |
6 | HG01993.hp1 HG02004.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.884-2117_884-2112d others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(1): Show |
10 | a0001c0001t0001g0091 a0001c0001t0002g0014 a0001c0001t0002g0129 others(7): Show |
10 | HG00408.hp1 HG01516.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.884-2119_884-2112d others(10): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(3): Show |
26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(23): Show |
26 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.884-2121_884-2112d others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(5): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0079 others(15): Show |
19 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.884-2123_884-2112d others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(7): Show |
9 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0236 others(6): Show |
9 | HG00733.hp1 HG01070.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-2125_884-2112d others(16): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(9): Show |
13 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0225 others(10): Show |
13 | HG00597.hp2 HG00621.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.884-2127_884-2112d others(18): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(11): Show |
12 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
14 | HG02129.hp2 HG02683.hp1 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.884-2129_884-2112d others(20): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(13): Show |
11 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0230 others(8): Show |
11 | HG00140.hp1 HG01433.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.884-2131_884-2112d others(22): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | AACACACA others(15): Show |
1 | a0001c0001t0002g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.884-2133_884-2112d others(24): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.884-2153_884-2152i others(13): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742954 | |||||||
| chr6:50742954 | A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0256 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.884-2153_884-2152i others(17): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742954 | |||||||
| chr6:50742954 | A | ACACACAC others(10): Show |
1 | a0001c0001t0002g0267 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.884-2153_884-2152i others(19): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742954 | |||||||
| chr6:50742954 | A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.884-2153_884-2152i others(21): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50742954 | |||||||
| chr6:50742954 | AAC | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(22): Show |
27 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.884-2113_884-2112d others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | AACAC | A | 41 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0075 others(38): Show |
42 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.884-2115_884-2112d others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
10 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.884-2121_884-2112d others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | AACACACA others(5): Show |
A | 15 | a0001c0001t0001g0030 a0001c0001t0003g0017 a0001c0001t0003g0018 others(12): Show |
15 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.884-2123_884-2112d others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50742954 | AACACACA others(7): Show |
A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-2125_884-2112d others(16): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50742954 | ||||||
| chr6:50743004 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.884-2103C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743004 | |||||||
| chr6:50743108 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.884-1999C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743108 | |||||||
| chr6:50743135 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0112 |
3 | HG02486.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.884-1972A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743135 | |||||||
| chr6:50743336 | A | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0170 |
2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.884-1771A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743336 | |||||||
| chr6:50743346 | A | T | 1 | a0002c0002t0001g0306 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.884-1761A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743346 | |||||||
| chr6:50743355 | A | ATTTTG | 84 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0002g0002 others(81): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.884-1713_884-1709d others(7): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50743355 | ||||||
| chr6:50743355 | A | ATTTTGTT others(3): Show |
2 | a0001c0001t0002g0312 a0001c0001t0004g0071 |
2 | HG01361.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.884-1718_884-1709d others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50743355 | ||||||
| chr6:50743355 | ATTTTG | A | 66 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0073 others(63): Show |
68 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.884-1713_884-1709d others(7): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50743355 | ||||||
| chr6:50743355 | ATTTTGTT others(3): Show |
A | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-1718_884-1709d others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50743355 | ||||||
| chr6:50743355 | ATTTTGTT others(13): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.884-1728_884-1709d others(22): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50743355 | ||||||
| chr6:50743614 | G | A | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.884-1493G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743614 | |||||||
| chr6:50743663 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.884-1444C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743663 | |||||||
| chr6:50743720 | A | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.884-1387A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743720 | |||||||
| chr6:50743837 | G | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-1270G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50743837 | |||||||
| chr6:50744008 | G | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-1099G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744008 | |||||||
| chr6:50744124 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.884-983G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744124 | |||||||
| chr6:50744170 | A | G | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.884-937A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744170 | |||||||
| chr6:50744223 | A | G | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-884A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744223 | |||||||
| chr6:50744301 | C | T | 22 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0003g0004 others(19): Show |
23 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.884-806C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744301 | |||||||
| chr6:50744344 | C | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.884-763C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744344 | |||||||
| chr6:50744402 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(24): Show |
28 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.884-705G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744402 | |||||||
| chr6:50744425 | A | AGAAAACT others(315): Show |
2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.884-666_884-665ins others(322): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 50744425 | ||||||
| chr6:50744667 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.884-440T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744667 | |||||||
| chr6:50744695 | T | A | 1 | a0001c0001t0002g0238 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.884-412T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744695 | |||||||
| chr6:50744795 | A | G | 275 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(272): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.884-312A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744795 | |||||||
| chr6:50744850 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
6 | HG02630.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.884-257T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744850 | |||||||
| chr6:50744959 | C | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(23): Show |
27 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.884-148C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744959 | |||||||
| chr6:50744979 | G | T | 11 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0039 others(8): Show |
12 | HG01891.hp2 HG01934.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.884-128G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50744979 | |||||||
| chr6:50745059 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.884-48T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50745059 | |||||||
| chr6:50745071 | A | G | 146 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(143): Show |
157 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.884-36A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 5/7 | chr6 | 50745071 | |||||||
| chr6:50745268 | C | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1025+20C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50745268 | |||||||
| chr6:50745302 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
6 | HG02630.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+54A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50745302 | |||||||
| chr6:50745677 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1025+429G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50745677 | |||||||
| chr6:50745729 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1025+481C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50745729 | |||||||
| chr6:50745785 | C | CT | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025+547dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 50745785 | ||||||
| chr6:50745933 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1025+685A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50745933 | |||||||
| chr6:50746029 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0232 a0001c0001t0003g0308 |
4 | NA18948.hp2 NA19063.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+781C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746029 | |||||||
| chr6:50746037 | A | C | 1 | a0001c0001t0004g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1025+789A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746037 | |||||||
| chr6:50746151 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+903A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746151 | |||||||
| chr6:50746227 | T | TTTTG | 73 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0002 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1025+1004_1025+100 others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 50746227 | ||||||
| chr6:50746227 | T | TTTTGTTT others(1): Show |
4 | a0001c0001t0002g0248 a0001c0001t0003g0059 a0001c0001t0003g0060 others(1): Show |
4 | HG02970.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+1000_1025+100 others(12): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 50746227 | ||||||
| chr6:50746227 | TTTTG | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1004_1025+100 others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 50746227 | ||||||
| chr6:50746269 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1025+1021C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746269 | |||||||
| chr6:50746373 | G | C | 1 | a0001c0001t0003g0224 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1025+1125G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746373 | |||||||
| chr6:50746443 | G | T | 5 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
5 | HG02280.hp2 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+1195G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746443 | |||||||
| chr6:50746457 | C | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01069.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+1209C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746457 | |||||||
| chr6:50746465 | T | C | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1025+1217T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746465 | |||||||
| chr6:50746569 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1025+1321G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746569 | |||||||
| chr6:50746769 | G | T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1025+1521G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50746769 | |||||||
| chr6:50747095 | G | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
10 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+1847G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747095 | |||||||
| chr6:50747133 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1025+1885G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747133 | |||||||
| chr6:50747538 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1025+2290A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747538 | |||||||
| chr6:50747548 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1025+2300C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747548 | |||||||
| chr6:50747659 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG00741.hp2 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+2411T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747659 | |||||||
| chr6:50747694 | C | T | 252 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(249): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1025+2446C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747694 | |||||||
| chr6:50747715 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1025+2467G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747715 | |||||||
| chr6:50747798 | G | T | 4 | a0001c0001t0003g0101 a0001c0001t0003g0104 a0001c0001t0003g0105 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+2550G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747798 | |||||||
| chr6:50747885 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0195 |
2 | HG00639.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1025+2637G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50747885 | |||||||
| chr6:50748052 | T | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1025+2804T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748052 | |||||||
| chr6:50748106 | T | C | 1 | a0001c0001t0006g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1025+2858T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748106 | |||||||
| chr6:50748263 | C | T | 7 | a0001c0001t0003g0051 a0001c0001t0003g0057 a0001c0003t0001g0081 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-2948C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748263 | |||||||
| chr6:50748270 | G | C | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1026-2941G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748270 | |||||||
| chr6:50748498 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1026-2713C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748498 | |||||||
| chr6:50748545 | T | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0180 a0001c0001t0001g0199 |
3 | HG01934.hp2 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1026-2666T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748545 | |||||||
| chr6:50748679 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0146 |
2 | HG01515.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1026-2532A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50748679 | |||||||
| chr6:50749276 | G | A | 4 | a0001c0001t0001g0135 a0001c0001t0003g0124 a0001c0001t0003g0125 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1935G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749276 | |||||||
| chr6:50749361 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG00280.hp2 HG00642.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-1850A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749361 | |||||||
| chr6:50749511 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1026-1700T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749511 | |||||||
| chr6:50749750 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1026-1461A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749750 | |||||||
| chr6:50749887 | G | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1026-1324G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749887 | |||||||
| chr6:50749897 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1026-1314A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50749897 | |||||||
| chr6:50750069 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1026-1142T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50750069 | |||||||
| chr6:50750227 | C | G | 1 | a0002c0002t0001g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1026-984C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50750227 | |||||||
| chr6:50750439 | G | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01069.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-772G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50750439 | |||||||
| chr6:50750609 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1026-602C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50750609 | |||||||
| chr6:50750978 | C | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(24): Show |
28 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.1026-233C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50750978 | |||||||
| chr6:50751025 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1026-186C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50751025 | |||||||
| chr6:50751026 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1026-185G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50751026 | |||||||
| chr6:50751042 | C | A | 1 | a0001c0001t0002g0230 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1026-169C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 6/7 | chr6 | 50751042 | |||||||
| chr6:50751457 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1139+133C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751457 | |||||||
| chr6:50751467 | T | C | 1 | a0001c0003t0001g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1139+143T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751467 | |||||||
| chr6:50751519 | C | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1139+195C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751519 | |||||||
| chr6:50751539 | G | C | 1 | a0001c0001t0002g0248 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1139+215G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751539 | |||||||
| chr6:50751634 | C | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1139+310C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751634 | |||||||
| chr6:50751655 | G | A | 11 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0039 others(8): Show |
12 | HG01891.hp2 HG01934.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139+331G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751655 | |||||||
| chr6:50751743 | T | G | 1 | a0002c0002t0001g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1139+419T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751743 | |||||||
| chr6:50751837 | T | A | 1 | a0001c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1139+513T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751837 | |||||||
| chr6:50751839 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1139+515A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751839 | |||||||
| chr6:50751891 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1139+567C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751891 | |||||||
| chr6:50751902 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1139+578G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50751902 | |||||||
| chr6:50752229 | A | T | 15 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0001g0152 others(12): Show |
15 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.1139+905A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752229 | |||||||
| chr6:50752526 | G | A | 7 | a0001c0001t0003g0051 a0001c0001t0003g0057 a0001c0003t0001g0081 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+1202G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752526 | |||||||
| chr6:50752571 | T | C | 1 | a0001c0001t0002g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1139+1247T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752571 | |||||||
| chr6:50752593 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1139+1269T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752593 | |||||||
| chr6:50752768 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1139+1444A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752768 | |||||||
| chr6:50752853 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1139+1529T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752853 | |||||||
| chr6:50752904 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1139+1580T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50752904 | |||||||
| chr6:50753132 | T | A | 3 | a0002c0002t0001g0286 a0002c0002t0001g0300 a0002c0002t0001g0302 |
3 | HG02135.hp2 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1139+1808T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753132 | |||||||
| chr6:50753353 | G | T | 21 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(18): Show |
21 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.1139+2029G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753353 | |||||||
| chr6:50753436 | T | C | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+2112T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753436 | |||||||
| chr6:50753524 | C | A | 1 | a0001c0001t0002g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1139+2200C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753524 | |||||||
| chr6:50753529 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1139+2205T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753529 | |||||||
| chr6:50753537 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139+2213A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753537 | |||||||
| chr6:50753595 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1139+2271C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753595 | |||||||
| chr6:50753612 | A | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1139+2288A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50753612 | |||||||
| chr6:50753614 | AGT | A | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+2292_1139+229 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50753614 | ||||||
| chr6:50754154 | C | A | 9 | a0001c0001t0004g0027 a0001c0001t0004g0072 a0001c0001t0004g0083 others(6): Show |
9 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139+2830C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754154 | |||||||
| chr6:50754223 | T | C | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1139+2899T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754223 | |||||||
| chr6:50754332 | C | CTG | 8 | a0001c0001t0001g0108 a0001c0001t0003g0040 a0001c0001t0003g0043 others(5): Show |
8 | HG01123.hp2 HG02280.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1139+3018_1139+301 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50754332 | ||||||
| chr6:50754559 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0183 |
2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1139+3235G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754559 | |||||||
| chr6:50754637 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1139+3313T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754637 | |||||||
| chr6:50754678 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
10 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1139+3354G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754678 | |||||||
| chr6:50754744 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(24): Show |
28 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.1139+3420T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50754744 | |||||||
| chr6:50755322 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1139+3998C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755322 | |||||||
| chr6:50755429 | T | TA | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(144): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1139+4121dupA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50755429 | ||||||
| chr6:50755429 | T | TAA | 27 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0080 others(24): Show |
28 | HG00408.hp2 HG00597.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1139+4120_1139+412 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50755429 | ||||||
| chr6:50755429 | TA | T | 8 | a0001c0001t0002g0128 a0001c0001t0002g0235 a0001c0001t0002g0265 others(5): Show |
8 | HG01258.hp1 HG01433.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1139+4121delA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50755429 | ||||||
| chr6:50755489 | A | G | 1 | a0001c0001t0003g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1139+4165A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755489 | |||||||
| chr6:50755502 | C | T | 8 | a0001c0001t0001g0108 a0001c0001t0003g0040 a0001c0001t0003g0043 others(5): Show |
8 | HG01123.hp2 HG02280.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1139+4178C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755502 | |||||||
| chr6:50755556 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0103 |
3 | HG03017.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1139+4232A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755556 | |||||||
| chr6:50755579 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1139+4255G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755579 | |||||||
| chr6:50755690 | T | C | 1 | a0001c0003t0001g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1139+4366T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755690 | |||||||
| chr6:50755832 | A | G | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+4508A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755832 | |||||||
| chr6:50755877 | T | C | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1139+4553T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755877 | |||||||
| chr6:50755912 | T | G | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+4588T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755912 | |||||||
| chr6:50755928 | T | C | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+4604T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50755928 | |||||||
| chr6:50756212 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1139+4888C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756212 | |||||||
| chr6:50756377 | CTAAT | C | 23 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0099 others(20): Show |
24 | HG00408.hp2 HG00597.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1139+5057_1139+506 others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50756377 | ||||||
| chr6:50756389 | A | T | 1 | a0001c0001t0002g0240 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1139+5065A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756389 | |||||||
| chr6:50756623 | C | A | 5 | a0002c0002t0001g0275 a0002c0002t0001g0281 a0002c0002t0001g0287 others(2): Show |
5 | HG02074.hp2 NA18982.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139+5299C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756623 | |||||||
| chr6:50756707 | G | A | 1 | a0001c0001t0003g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1139+5383G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756707 | |||||||
| chr6:50756897 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0198 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1139+5573T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756897 | |||||||
| chr6:50756956 | G | T | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+5632G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50756956 | |||||||
| chr6:50757038 | T | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1139+5714T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757038 | |||||||
| chr6:50757140 | C | A | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1139+5816C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757140 | |||||||
| chr6:50757210 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1139+5886C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757210 | |||||||
| chr6:50757294 | GATATTCT others(2): Show |
G | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139+5992_1139+600 others(13): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757294 | ||||||
| chr6:50757325 | G | GAT | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+6010_1139+601 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757325 | ||||||
| chr6:50757416 | CTATATAG others(4): Show |
C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1139+6110_1139+612 others(15): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757416 | ||||||
| chr6:50757434 | G | GAATATAT others(21): Show |
5 | a0001c0001t0002g0223 a0001c0001t0002g0242 a0001c0001t0002g0259 others(2): Show |
5 | HG01070.hp1 HG02074.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139+6120_1139+612 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757434 | ||||||
| chr6:50757434 | G | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(102): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1139+6110G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757434 | |||||||
| chr6:50757445 | C | A | 192 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(189): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1139+6121C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757445 | |||||||
| chr6:50757451 | CTA | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01433.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1139+6138_1139+613 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757451 | ||||||
| chr6:50757453 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1139+6140_1139+616 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757453 | ||||||
| chr6:50757462 | T | A | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1139+6138T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757462 | |||||||
| chr6:50757462 | T | TAATATAT others(21): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02080.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1139+6163_1139+616 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757462 | ||||||
| chr6:50757467 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1139+6143T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757467 | |||||||
| chr6:50757467 | TATATAAT others(75): Show |
T | 1 | a0001c0001t0003g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1139+6166_1139+624 others(86): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757467 | ||||||
| chr6:50757473 | A | C | 1 | a0001c0005t0001g0278 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1139+6149A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757473 | |||||||
| chr6:50757479 | CTA | C | 10 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1139+6166_1139+616 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757479 | ||||||
| chr6:50757481 | ATATATAT others(19): Show |
A | 10 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0001g0147 others(7): Show |
10 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1139+6166_1139+619 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757481 | ||||||
| chr6:50757490 | T | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1139+6166T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757490 | |||||||
| chr6:50757495 | T | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(99): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1139+6171T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757495 | |||||||
| chr6:50757495 | T | TATATAAT others(19): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0199 |
2 | HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1139+6192_1139+621 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757495 | ||||||
| chr6:50757507 | C | CTA | 76 | a0001c0001t0001g0097 a0001c0001t0001g0171 a0001c0001t0001g0172 others(73): Show |
85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1139+6190_1139+619 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757507 | ||||||
| chr6:50757507 | C | CTATATAT others(21): Show |
1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1139+6225_1139+625 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757507 | ||||||
| chr6:50757507 | C | CTATATAT others(49): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01069.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+6197_1139+625 others(60): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757507 | ||||||
| chr6:50757507 | CTATATAT others(21): Show |
C | 3 | a0001c0001t0001g0030 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02630.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+6225_1139+625 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757507 | ||||||
| chr6:50757516 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(62): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1139+6192G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757516 | |||||||
| chr6:50757521 | C | CATATAAT others(21): Show |
9 | a0001c0001t0001g0120 a0001c0001t0002g0055 a0001c0001t0003g0069 others(6): Show |
9 | HG00140.hp2 HG01074.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1139+6224_1139+622 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757521 | ||||||
| chr6:50757521 | C | CATATAAT others(49): Show |
1 | a0001c0001t0001g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1139+6224_1139+622 others(60): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757521 | ||||||
| chr6:50757521 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(62): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1139+6197C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757521 | |||||||
| chr6:50757533 | CTA | C | 74 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0001g0147 others(71): Show |
81 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1139+6218_1139+621 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757533 | ||||||
| chr6:50757535 | A | ATATATAT others(19): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0130 |
3 | HG00438.hp1 HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1139+6219_1139+622 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757535 | ||||||
| chr6:50757535 | A | ATATATAT others(47): Show |
1 | a0001c0001t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1139+6219_1139+622 others(58): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757535 | ||||||
| chr6:50757549 | C | CATATAAT others(21): Show |
12 | a0001c0001t0001g0036 a0001c0001t0001g0110 a0001c0001t0001g0120 others(9): Show |
12 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1139+6386_1139+641 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757549 | ||||||
| chr6:50757549 | C | CATATAAT others(49): Show |
1 | a0002c0002t0001g0298 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1139+6358_1139+641 others(60): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757549 | ||||||
| chr6:50757549 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(113): Show |
121 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.1139+6225C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757549 | |||||||
| chr6:50757549 | CATATAAT others(21): Show |
C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1139+6386_1139+641 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757549 | ||||||
| chr6:50757549 | CATATAAT others(49): Show |
C | 1 | a0001c0001t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1139+6358_1139+641 others(60): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757549 | ||||||
| chr6:50757549 | CATATAAT others(105): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1139+6302_1139+641 others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757549 | ||||||
| chr6:50757577 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(24): Show |
29 | HG01069.hp2 HG01123.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1139+6253T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757577 | |||||||
| chr6:50757589 | C | CTATATAT others(14): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139+6266_1139+628 others(25): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757589 | ||||||
| chr6:50757598 | T | TAGAATAT others(48): Show |
1 | a0001c0001t0003g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1139+6288_1139+628 others(59): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757598 | ||||||
| chr6:50757605 | T | C | 7 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG01123.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+6281T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757605 | |||||||
| chr6:50757611 | AT | A | 3 | a0001c0001t0003g0101 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02055.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1139+6289delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757611 | ||||||
| chr6:50757626 | T | G | 1 | a0001c0001t0003g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1139+6302T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757626 | |||||||
| chr6:50757640 | T | A | 1 | a0001c0001t0002g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1139+6316T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757640 | |||||||
| chr6:50757654 | T | G | 1 | a0001c0001t0003g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1139+6330T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757654 | |||||||
| chr6:50757675 | ATATATAT others(47): Show |
A | 1 | a0002c0002t0001g0299 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1139+6414_1139+646 others(58): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757675 | ||||||
| chr6:50757682 | T | G | 3 | a0001c0001t0003g0101 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02055.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1139+6358T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757682 | |||||||
| chr6:50757695 | AT | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1139+6373delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757695 | ||||||
| chr6:50757701 | CTA | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
12 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139+6386_1139+638 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757701 | ||||||
| chr6:50757701 | CTATATAT others(98): Show |
C | 2 | a0001c0001t0003g0004 a0001c0001t0003g0039 |
3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1139+6404_1139+650 others(4): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757701 | ||||||
| chr6:50757703 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1139+6414_1139+643 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757703 | ||||||
| chr6:50757729 | C | CTA | 119 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1139+6412_1139+641 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757729 | ||||||
| chr6:50757729 | C | CTATATAT others(21): Show |
7 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0150 others(4): Show |
7 | HG03492.hp2 NA18946.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139+6458_1139+648 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757729 | ||||||
| chr6:50757729 | C | CTATATAT others(49): Show |
1 | a0001c0001t0001g0304 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1139+6430_1139+648 others(60): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757729 | ||||||
| chr6:50757729 | CTATATAT others(21): Show |
C | 1 | a0001c0001t0002g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1139+6458_1139+648 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757729 | ||||||
| chr6:50757729 | CTATATAT others(70): Show |
C | 7 | a0001c0001t0003g0041 a0001c0001t0003g0048 a0001c0001t0003g0049 others(4): Show |
7 | HG01934.hp1 HG02602.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+6414_1139+649 others(81): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757729 | ||||||
| chr6:50757750 | T | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
16 | HG00741.hp2 HG01123.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1139+6426T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757750 | |||||||
| chr6:50757755 | C | CTATATAT others(44): Show |
1 | a0001c0001t0003g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1139+6453_1139+645 others(55): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757755 | ||||||
| chr6:50757755 | CTA | C | 22 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0002g0239 others(19): Show |
22 | HG00621.hp2 HG00733.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1139+6440_1139+644 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757755 | ||||||
| chr6:50757755 | CTATATAT others(44): Show |
C | 4 | a0001c0001t0003g0037 a0001c0001t0003g0042 a0001c0001t0003g0047 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+6458_1139+650 others(55): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757755 | ||||||
| chr6:50757757 | A | ATATATAG others(17): Show |
3 | a0001c0003t0001g0098 a0001c0003t0001g0102 a0001c0003t0001g0107 |
3 | HG02559.hp2 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1139+6439_1139+644 others(28): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757757 | ||||||
| chr6:50757757 | A | ATATATAT others(19): Show |
65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(62): Show |
73 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1139+6442_1139+646 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757757 | ||||||
| chr6:50757757 | A | ATATATAT others(47): Show |
4 | a0001c0001t0002g0003 a0001c0001t0003g0101 a0001c0001t0003g0105 others(1): Show |
4 | HG00438.hp1 HG02055.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139+6485_1139+648 others(58): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757757 | ||||||
| chr6:50757771 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1139+6447T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757771 | |||||||
| chr6:50757778 | T | A | 29 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(26): Show |
29 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1139+6454T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757778 | |||||||
| chr6:50757778 | T | TTATTCTA others(19): Show |
1 | a0001c0003t0001g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1139+6467_1139+646 others(30): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757778 | ||||||
| chr6:50757778 | T | TTATTCTA others(45): Show |
3 | a0001c0001t0003g0022 a0001c0001t0003g0057 a0001c0003t0001g0301 |
3 | HG02615.hp2 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1139+6467_1139+646 others(56): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757778 | ||||||
| chr6:50757778 | T | TTATTCTA others(21): Show |
9 | a0001c0001t0004g0027 a0001c0001t0004g0072 a0001c0001t0004g0083 others(6): Show |
9 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139+6481_1139+648 others(32): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757778 | ||||||
| chr6:50757778 | T | TTATTCTA others(73): Show |
4 | a0001c0001t0003g0017 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+6485_1139+648 others(84): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757778 | ||||||
| chr6:50757783 | C | CTATATAT others(16): Show |
1 | a0002c0002t0001g0290 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1139+6493_1139+651 others(27): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757783 | ||||||
| chr6:50757783 | CTATATAT others(16): Show |
C | 1 | a0001c0001t0003g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1139+6493_1139+651 others(27): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757783 | ||||||
| chr6:50757794 | G | GAATATAT others(38): Show |
1 | a0001c0001t0001g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1139+6479_1139+652 others(49): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757794 | ||||||
| chr6:50757806 | T | TTATTC | 4 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0002g0312 others(1): Show |
4 | HG01515.hp1 HG02683.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+6485_1139+648 others(9): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757806 | ||||||
| chr6:50757806 | T | TTATTCTA others(50): Show |
2 | a0001c0001t0003g0021 a0001c0001t0003g0112 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1139+6485_1139+648 others(61): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757806 | ||||||
| chr6:50757815 | T | TAGAATAT others(16): Show |
2 | a0001c0001t0003g0021 a0001c0001t0003g0112 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1139+6513_1139+651 others(27): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757815 | ||||||
| chr6:50757815 | T | TAGAATAT others(96): Show |
1 | a0001c0001t0003g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1139+6508_1139+650 others(107): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50757815 | ||||||
| chr6:50757951 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG00280.hp2 HG00642.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139+6627C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757951 | |||||||
| chr6:50757952 | G | T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+6628G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757952 | |||||||
| chr6:50757958 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1139+6634T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50757958 | |||||||
| chr6:50758051 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1139+6727C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758051 | |||||||
| chr6:50758399 | T | C | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1139+7075T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758399 | |||||||
| chr6:50758461 | C | G | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139+7137C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758461 | |||||||
| chr6:50758466 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1139+7142C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758466 | |||||||
| chr6:50758540 | G | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0022 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+7216G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758540 | |||||||
| chr6:50758549 | G | A | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+7225G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758549 | |||||||
| chr6:50758774 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0047 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1139+7450A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50758774 | |||||||
| chr6:50759310 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1139+7986C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759310 | |||||||
| chr6:50759358 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1139+8034T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759358 | |||||||
| chr6:50759602 | T | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0213 |
2 | HG02080.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1139+8278T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759602 | |||||||
| chr6:50759603 | G | A | 3 | a0002c0002t0001g0270 a0002c0002t0001g0283 a0002c0002t0001g0299 |
3 | HG00621.hp1 HG02040.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1139+8279G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759603 | |||||||
| chr6:50759668 | A | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 |
3 | HG02818.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1139+8344A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759668 | |||||||
| chr6:50759857 | G | A | 102 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(99): Show |
112 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1139+8533G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50759857 | |||||||
| chr6:50760035 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1139+8711C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760035 | |||||||
| chr6:50760054 | T | C | 7 | a0001c0001t0002g0129 a0001c0001t0002g0228 a0001c0001t0002g0229 others(4): Show |
7 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139+8730T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760054 | |||||||
| chr6:50760227 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1139+8903C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760227 | |||||||
| chr6:50760326 | T | C | 1 | a0002c0002t0001g0296 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1139+9002T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760326 | |||||||
| chr6:50760368 | T | G | 11 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0039 others(8): Show |
12 | HG01891.hp2 HG01934.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139+9044T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760368 | |||||||
| chr6:50760415 | A | C | 103 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(100): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1139+9091A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760415 | |||||||
| chr6:50760587 | G | A | 7 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG01123.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139+9263G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760587 | |||||||
| chr6:50760909 | C | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
10 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1139+9585C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50760909 | |||||||
| chr6:50761033 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1139+9709G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761033 | |||||||
| chr6:50761199 | C | G | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1139+9875C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761199 | |||||||
| chr6:50761228 | C | CA | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(93): Show |
105 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1139+9915dupA | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50761228 | ||||||
| chr6:50761441 | G | T | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139+10117G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761441 | |||||||
| chr6:50761509 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1139+10185T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761509 | |||||||
| chr6:50761521 | A | T | 1 | a0001c0001t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1139+10197A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761521 | |||||||
| chr6:50761977 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1139+10653T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50761977 | |||||||
| chr6:50762082 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0160 |
2 | NA18946.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1140-10563A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762082 | |||||||
| chr6:50762106 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1140-10539G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762106 | |||||||
| chr6:50762242 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1140-10403A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762242 | |||||||
| chr6:50762444 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(24): Show |
28 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.1140-10201A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762444 | |||||||
| chr6:50762461 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1140-10184C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762461 | |||||||
| chr6:50762574 | T | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG00280.hp2 HG00642.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1140-10071T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50762574 | |||||||
| chr6:50763022 | C | G | 146 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(143): Show |
157 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1140-9623C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50763022 | |||||||
| chr6:50763029 | ATCT | A | 4 | a0001c0001t0001g0155 a0001c0001t0001g0167 a0001c0001t0001g0202 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-9608_1140-960 others(7): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50763029 | ||||||
| chr6:50763179 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1140-9466T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50763179 | |||||||
| chr6:50763272 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1140-9373C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50763272 | |||||||
| chr6:50763656 | T | TG | 5 | a0001c0001t0001g0138 a0001c0001t0001g0166 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140-8987dupG | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50763656 | ||||||
| chr6:50764003 | A | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0001g0152 others(5): Show |
8 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140-8642A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764003 | |||||||
| chr6:50764113 | C | T | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0133 |
3 | HG02451.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1140-8532C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764113 | |||||||
| chr6:50764222 | C | T | 5 | a0001c0001t0002g0016 a0001c0001t0002g0251 a0001c0001t0002g0252 others(2): Show |
5 | NA18955.hp2 NA18994.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140-8423C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764222 | |||||||
| chr6:50764419 | C | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01069.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-8226C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764419 | |||||||
| chr6:50764600 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1140-8045G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764600 | |||||||
| chr6:50764658 | C | A | 1 | a0002c0002t0001g0299 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1140-7987C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764658 | |||||||
| chr6:50764929 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1140-7716A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50764929 | |||||||
| chr6:50765248 | T | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00544.hp2 HG00673.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1140-7397T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765248 | |||||||
| chr6:50765372 | T | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(80): Show |
92 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1140-7273T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765372 | |||||||
| chr6:50765441 | T | C | 8 | a0001c0001t0001g0108 a0001c0001t0003g0040 a0001c0001t0003g0043 others(5): Show |
8 | HG01123.hp2 HG02280.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140-7204T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765441 | |||||||
| chr6:50765463 | G | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0097 others(110): Show |
123 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1140-7182G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765463 | |||||||
| chr6:50765556 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1140-7089T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765556 | |||||||
| chr6:50765719 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
6 | HG02630.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140-6926T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765719 | |||||||
| chr6:50765935 | A | T | 146 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(143): Show |
157 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1140-6710A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50765935 | |||||||
| chr6:50766003 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1140-6642C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766003 | |||||||
| chr6:50766035 | G | C | 1 | a0001c0001t0003g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1140-6610G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766035 | |||||||
| chr6:50766063 | C | A | 98 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0108 others(95): Show |
108 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1140-6582C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766063 | |||||||
| chr6:50766118 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1140-6527A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766118 | |||||||
| chr6:50766446 | T | A | 1 | a0001c0001t0003g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1140-6199T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766446 | |||||||
| chr6:50766481 | A | G | 19 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(16): Show |
19 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1140-6164A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766481 | |||||||
| chr6:50766560 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1140-6085A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766560 | |||||||
| chr6:50766654 | C | CT | 12 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0090 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140-5966dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTT | 18 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG01069.hp2 HG01934.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1140-5967_1140-596 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
27 | HG00733.hp2 HG00741.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1140-5968_1140-596 others(7): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTT | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0028 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140-5969_1140-596 others(8): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTT | 22 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0118 others(19): Show |
23 | HG01361.hp1 HG01978.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.1140-5970_1140-596 others(9): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0229 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1140-5975_1140-596 others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(10): Show |
14 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0053 others(11): Show |
17 | HG01069.hp1 HG01070.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1140-5982_1140-596 others(21): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(11): Show |
20 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0128 others(17): Show |
22 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1140-5983_1140-596 others(22): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0234 a0001c0001t0002g0237 a0001c0001t0002g0245 |
3 | HG00438.hp2 HG00621.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1140-5984_1140-596 others(23): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0002g0223 a0001c0001t0002g0240 a0001c0001t0002g0254 others(1): Show |
4 | HG00544.hp1 HG02165.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140-5985_1140-596 others(24): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0002g0014 a0001c0001t0002g0235 a0001c0001t0002g0251 |
4 | NA18960.hp1 NA18999.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-5986_1140-596 others(25): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(15): Show |
10 | a0001c0001t0002g0016 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
10 | HG00408.hp1 HG00673.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1140-5987_1140-596 others(26): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0002g0253 a0003c0004t0002g0247 |
2 | HG01192.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1140-5988_1140-596 others(27): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | CTTT | C | 6 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0015 others(3): Show |
9 | HG01192.hp2 HG06807.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1140-5968_1140-596 others(7): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | CTTTTTTT others(3): Show |
C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(25): Show |
29 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1140-5975_1140-596 others(14): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766654 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1140-5976_1140-596 others(15): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50766654 | ||||||
| chr6:50766770 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1140-5875G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766770 | |||||||
| chr6:50766813 | T | C | 71 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(68): Show |
80 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1140-5832T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766813 | |||||||
| chr6:50766825 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1140-5820C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766825 | |||||||
| chr6:50766963 | C | T | 5 | a0001c0003t0001g0081 a0001c0003t0001g0098 a0001c0003t0001g0102 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140-5682C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50766963 | |||||||
| chr6:50767042 | C | T | 74 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(71): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1140-5603C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767042 | |||||||
| chr6:50767248 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1140-5397G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767248 | |||||||
| chr6:50767271 | A | G | 99 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0108 others(96): Show |
109 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1140-5374A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767271 | |||||||
| chr6:50767293 | T | A | 1 | a0001c0001t0003g0111 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140-5352T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767293 | |||||||
| chr6:50767433 | T | C | 74 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(71): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1140-5212T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767433 | |||||||
| chr6:50767824 | A | G | 99 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0108 others(96): Show |
109 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1140-4821A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767824 | |||||||
| chr6:50767943 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1140-4702A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50767943 | |||||||
| chr6:50768052 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0167 a0001c0001t0001g0202 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-4593C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768052 | |||||||
| chr6:50768150 | T | A | 74 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(71): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1140-4495T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768150 | |||||||
| chr6:50768215 | AT | A | 38 | a0001c0001t0001g0120 a0001c0001t0001g0149 a0001c0001t0001g0171 others(35): Show |
38 | HG00140.hp2 HG00621.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1140-4414delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768215 | ||||||
| chr6:50768219 | T | A | 95 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0108 others(92): Show |
105 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1140-4426T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768219 | |||||||
| chr6:50768220 | T | A | 4 | a0001c0003t0001g0081 a0001c0003t0001g0098 a0001c0003t0001g0102 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-4425T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768220 | |||||||
| chr6:50768223 | T | A | 74 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(71): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1140-4422T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768223 | |||||||
| chr6:50768273 | C | CT | 84 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(81): Show |
93 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1140-4356dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768273 | ||||||
| chr6:50768273 | CT | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(18): Show |
22 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1140-4356delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768273 | ||||||
| chr6:50768333 | CT | C | 94 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0173 others(91): Show |
104 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1140-4299delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768333 | ||||||
| chr6:50768514 | T | C | 1 | a0002c0002t0001g0290 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1140-4131T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768514 | |||||||
| chr6:50768812 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1140-3833G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768812 | |||||||
| chr6:50768895 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1140-3750C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768895 | |||||||
| chr6:50768903 | C | CT | 13 | a0001c0001t0001g0089 a0001c0001t0001g0103 a0001c0001t0001g0198 others(10): Show |
13 | HG01169.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1140-3725dupT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768903 | ||||||
| chr6:50768903 | C | CTT | 87 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0080 others(84): Show |
97 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1140-3726_1140-372 others(6): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768903 | ||||||
| chr6:50768903 | CT | C | 38 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
39 | HG00733.hp2 HG00741.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.1140-3725delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50768903 | ||||||
| chr6:50768965 | C | A | 4 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0282 others(1): Show |
4 | HG02155.hp2 NA18942.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140-3680C>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50768965 | |||||||
| chr6:50769058 | AT | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0115 others(6): Show |
11 | HG00280.hp2 HG00642.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1140-3577delT | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 50769058 | ||||||
| chr6:50769122 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(67): Show |
79 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1140-3523C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50769122 | |||||||
| chr6:50769140 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0108 others(96): Show |
109 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1140-3505T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50769140 | |||||||
| chr6:50769201 | G | T | 1 | a0001c0001t0003g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1140-3444G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50769201 | |||||||
| chr6:50770165 | T | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
6 | HG02630.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140-2480T>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770165 | |||||||
| chr6:50770192 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG02723.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140-2453G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770192 | |||||||
| chr6:50770206 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0177 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1140-2439A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770206 | |||||||
| chr6:50770240 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1140-2405G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770240 | |||||||
| chr6:50770242 | C | T | 1 | a0002c0002t0001g0277 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1140-2403C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770242 | |||||||
| chr6:50770273 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1140-2372T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770273 | |||||||
| chr6:50770314 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1140-2331A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770314 | |||||||
| chr6:50770357 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1140-2288T>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770357 | |||||||
| chr6:50770380 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1140-2265G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770380 | |||||||
| chr6:50770413 | A | AT | 81 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(78): Show |
90 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1140-2232_1140-223 others(5): Show |
TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770413 | |||||||
| chr6:50770414 | A | T | 105 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0173 others(102): Show |
115 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1140-2231A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770414 | |||||||
| chr6:50770447 | A | T | 1 | a0001c0001t0003g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1140-2198A>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770447 | |||||||
| chr6:50770512 | C | T | 7 | a0001c0001t0003g0051 a0001c0001t0003g0057 a0001c0003t0001g0081 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140-2133C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770512 | |||||||
| chr6:50770786 | G | C | 1 | a0001c0001t0004g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1140-1859G>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50770786 | |||||||
| chr6:50771206 | A | G | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1140-1439A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771206 | |||||||
| chr6:50771318 | G | A | 1 | a0003c0004t0002g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1140-1327G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771318 | |||||||
| chr6:50771361 | T | C | 81 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0002 others(78): Show |
90 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1140-1284T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771361 | |||||||
| chr6:50771530 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
5 | HG02280.hp2 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140-1115T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771530 | |||||||
| chr6:50771593 | G | A | 19 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(16): Show |
19 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1140-1052G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771593 | |||||||
| chr6:50771602 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1140-1043T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771602 | |||||||
| chr6:50771682 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1140-963A>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771682 | |||||||
| chr6:50771791 | G | T | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02970.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1140-854G>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771791 | |||||||
| chr6:50771864 | C | G | 1 | a0001c0001t0003g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1140-781C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771864 | |||||||
| chr6:50771929 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0001g0153 others(5): Show |
8 | HG02080.hp1 HG02129.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140-716C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771929 | |||||||
| chr6:50771936 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1140-709T>C | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50771936 | |||||||
| chr6:50772005 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1140-640A>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50772005 | |||||||
| chr6:50772229 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1140-416C>T | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50772229 | |||||||
| chr6:50772230 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1140-415G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50772230 | |||||||
| chr6:50772245 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1140-400G>A | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50772245 | |||||||
| chr6:50772250 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1140-395C>G | TFAP2D | ENSG00000008197.5 | transcript | ENST00000008391.4 | protein_coding | 7/7 | chr6 | 50772250 |