Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23643 |
| ensemblid | ENSG00000154589.7 |
| hgncid | 17156 |
| symbol | LY96 |
| name | lymphocyte antigen 96 |
| refseq_nuc | NM_015364.5 |
| refseq_prot | NP_056179.4 |
| ensembl_nuc | ENST00000284818.7 |
| ensembl_prot | ENSP00000284818.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 73991392 |
| end | 74029079 |
| strand | + |
| ver | v1.2 |
| region | chr8:73991392-74029079 |
| region5000 | chr8:73986392-74034079 |
| regionname0 | LY96_chr8_73991392_74029079 |
| regionname5000 | LY96_chr8_73986392_74034079 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 160 | 304 | 80 | 60 | 120 | 14 | 29 | 86 | LY96_chr8_73986392_74034079 | LY96 | MLPFL others(155): Show |
chr8 | 73986392 | 74034079 |
| a0002 | 1/0 | 160 | 4 | 1 | 1 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | MLPFL others(155): Show |
chr8 | 73986392 | 74034079 |
| a0003 | 0/0 | 160 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | MLPFL others(155): Show |
chr8 | 73986392 | 74034079 |
| a0004 | 0/0 | 121 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | MQYPI others(116): Show |
chr8 | 73986392 | 74034079 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 480 | 304 | 80 | 60 | 120 | 14 | 29 | LY96_chr8_73986392_74034079 | LY96 | ATGTT others(475): Show |
chr8 | 73986392 | 74034079 | ||
| a0002c0002 | 1/0 | 480 | 4 | 1 | 1 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | ATGTT others(475): Show |
chr8 | 73986392 | 74034079 | ||
| a0003c0004 | 0/0 | 480 | 3 | 0 | 3 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | ATGTT others(475): Show |
chr8 | 73986392 | 74034079 | ||
| a0004c0003 | 0/0 | 368 | 3 | 3 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | ATAAA others(363): Show |
chr8 | 73986392 | 74034079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 559 | 276 | 53 | 59 | 120 | 14 | 29 | LY96_chr8_73986392_74034079 | LY96 | GATTA others(554): Show |
chr8 | 73986392 | 74034079 |
| a0001c0001t0002 | 0/0 | 559 | 28 | 27 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | GATTA others(554): Show |
chr8 | 73986392 | 74034079 |
| a0002c0002t0001 | 1/0 | 559 | 4 | 1 | 1 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | GATTA others(554): Show |
chr8 | 73986392 | 74034079 |
| a0003c0004t0001 | 0/0 | 559 | 3 | 0 | 3 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | GATTA others(554): Show |
chr8 | 73986392 | 74034079 |
| a0004c0003t0003 | 0/0 | 396 | 3 | 3 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | ATAAA others(391): Show |
chr8 | 73986392 | 74034079 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0002c0002t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0003c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0003c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0003c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0004c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0004c0003t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| a0004c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00639 | hp2 | a0003 | c0004 | t0001 | g0059 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01106 | hp2 | a0003 | c0004 | t0001 | g0053 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01934 | hp1 | a0003 | c0004 | t0001 | g0108 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02615 | hp1 | a0004 | c0003 | t0003 | g0011 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02896 | hp2 | a0004 | c0003 | t0003 | g0012 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02897 | hp2 | a0004 | c0003 | t0003 | g0013 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ASW | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ASW | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | TSI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | GIH | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0043 | REF | REF | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0087 | REF | REF | LY96_chr8_73986392_74034079 | LY96 | chr8 | 73986392 | 74034079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:73991452 | T | A | 1 | a0001 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.10T>A | p.Phe4Ile | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/5 | 61/559 | 10/483 | 4/160 | chr8 | 73991452 | |||
| chr8:73991550 | C | G | 1 | a0001 | 1 | NA18988.hp1 | stop_gained | HIGH | c.108C>G | p.Tyr36* | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/5 | 159/559 | 108/483 | 36/160 | chr8 | 73991550 | |||
| chr8:74004849 | A | G | 3 | a0001 a0003 a0004 |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
missense_variant | MODERATE | c.166A>G | p.Arg56Gly | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/5 | 217/559 | 166/483 | 56/160 | chr8 | 74004849 | |||
| chr8:74029040 | C | T | 1 | a0003 | 3 | HG00639.hp2 HG01106.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.469C>T | p.Pro157Ser | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 5/5 | 520/559 | 469/483 | 157/160 | chr8 | 74029040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:73991526 | C | T | 1 | a0001c0001 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.84C>T | p.Ser28Ser | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/5 | 135/559 | 84/483 | 28/160 | chr8 | 73991526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:74029071 | A | C | 2 | a0001c0001t0002 a0004c0003t0003 |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 5/5 | 17 | chr8 | 74029071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:73991567 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.112+13G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73991567 | |||||||
| chr8:73991700 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+146A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73991700 | |||||||
| chr8:73991765 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+211T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73991765 | |||||||
| chr8:73991901 | T | C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(68): Show |
73 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.112+347T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73991901 | |||||||
| chr8:73992068 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.112+514A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992068 | |||||||
| chr8:73992134 | A | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0255 a0001c0001t0001g0256 others(46): Show |
50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+580A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992134 | |||||||
| chr8:73992472 | T | G | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112+918T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992472 | |||||||
| chr8:73992529 | G | C | 9 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+975G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992529 | |||||||
| chr8:73992542 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.112+988G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992542 | |||||||
| chr8:73992768 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112+1214C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992768 | |||||||
| chr8:73992781 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.112+1227G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992781 | |||||||
| chr8:73992836 | C | CTG | 14 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
14 | HG01109.hp1 HG01515.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+1321_112+1322d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTATGT others(1): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG00735.hp1 NA18951.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+1285_112+1286i others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTATGT others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.112+1285_112+1286i others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTG | 25 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0164 others(22): Show |
27 | HG00438.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.112+1319_112+1322d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTG | 19 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0186 others(16): Show |
21 | HG00408.hp1 HG02258.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.112+1317_112+1322d others(8): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(1): Show |
10 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(7): Show |
10 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+1315_112+1322d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(3): Show |
16 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(13): Show |
16 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.112+1313_112+1322d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(5): Show |
16 | a0001c0001t0001g0009 a0001c0001t0001g0228 a0001c0001t0001g0229 others(13): Show |
17 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.112+1311_112+1322d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00741.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.112+1309_112+1322d others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01993.hp2 HG02148.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.112+1307_112+1322d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(11): Show |
4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG01261.hp1 HG01981.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1305_112+1322d others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.112+1303_112+1322d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTG | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01109.hp2 HG02155.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+1321_112+1322d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTG | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01433.hp2 HG02572.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.112+1319_112+1322d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTGTG | C | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG02738.hp2 NA18941.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.112+1317_112+1322d others(8): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTGTGT others(1): Show |
C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0255 a0001c0001t0001g0256 others(43): Show |
47 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.112+1315_112+1322d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTGTGT others(9): Show |
C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+1307_112+1322d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTGTGT others(11): Show |
C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+1305_112+1322d others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992836 | CTGTGTGT others(13): Show |
C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112+1303_112+1322d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73992836 | ||||||
| chr8:73992875 | T | A | 1 | a0001c0001t0001g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.112+1321T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992875 | |||||||
| chr8:73992915 | C | T | 64 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(61): Show |
66 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.112+1361C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992915 | |||||||
| chr8:73992920 | T | G | 89 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(86): Show |
92 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.112+1366T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992920 | |||||||
| chr8:73992921 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG00735.hp1 HG04199.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+1367T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992921 | |||||||
| chr8:73992958 | G | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112+1404G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73992958 | |||||||
| chr8:73993021 | A | AT | 11 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0006 others(8): Show |
12 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.112+1481dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73993021 | ||||||
| chr8:73993252 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.112+1698T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993252 | |||||||
| chr8:73993391 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+1837T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993391 | |||||||
| chr8:73993528 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
19 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.112+1974C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993528 | |||||||
| chr8:73993529 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+1975G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993529 | |||||||
| chr8:73993535 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.112+1981T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993535 | |||||||
| chr8:73993685 | C | A | 1 | a0001c0001t0002g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+2131C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993685 | |||||||
| chr8:73993720 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.112+2166G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993720 | |||||||
| chr8:73993752 | A | T | 4 | a0001c0001t0001g0146 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | HG02055.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2198A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993752 | |||||||
| chr8:73993767 | T | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+2213T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993767 | |||||||
| chr8:73993793 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0002g0035 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.112+2239G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993793 | |||||||
| chr8:73993796 | C | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.112+2242C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993796 | |||||||
| chr8:73993822 | TC | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.112+2271delC | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73993822 | ||||||
| chr8:73993849 | G | A | 1 | a0003c0004t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.112+2295G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993849 | |||||||
| chr8:73993952 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.112+2398C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993952 | |||||||
| chr8:73993958 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.112+2404C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73993958 | |||||||
| chr8:73993988 | G | GT | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+2445dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73993988 | ||||||
| chr8:73994047 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.112+2493C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994047 | |||||||
| chr8:73994075 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG00735.hp1 HG04199.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+2521C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994075 | |||||||
| chr8:73994087 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.112+2533C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994087 | |||||||
| chr8:73994279 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.112+2725T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994279 | |||||||
| chr8:73994344 | G | C | 1 | a0001c0001t0002g0205 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112+2790G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994344 | |||||||
| chr8:73994487 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112+2933T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994487 | |||||||
| chr8:73994494 | A | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(67): Show |
72 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.112+2940A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994494 | |||||||
| chr8:73994632 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.112+3078G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994632 | |||||||
| chr8:73994716 | G | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.112+3162G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994716 | |||||||
| chr8:73994741 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.112+3187C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994741 | |||||||
| chr8:73994872 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+3318C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73994872 | |||||||
| chr8:73995014 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(14): Show |
18 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.112+3460A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995014 | |||||||
| chr8:73995052 | C | G | 13 | a0001c0001t0001g0044 a0001c0001t0001g0252 a0001c0001t0001g0253 others(10): Show |
14 | HG01109.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+3498C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995052 | |||||||
| chr8:73995060 | A | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0255 a0001c0001t0001g0256 others(33): Show |
37 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+3506A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995060 | |||||||
| chr8:73995290 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.112+3736C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995290 | |||||||
| chr8:73995323 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.112+3769C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995323 | |||||||
| chr8:73995365 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112+3811C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995365 | |||||||
| chr8:73995387 | C | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+3833C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995387 | |||||||
| chr8:73995555 | A | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.112+4001A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995555 | |||||||
| chr8:73995578 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(60): Show |
65 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+4024G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995578 | |||||||
| chr8:73995588 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.112+4034A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995588 | |||||||
| chr8:73995685 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.112+4131G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995685 | |||||||
| chr8:73995728 | A | AT | 68 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(65): Show |
70 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.112+4184dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73995728 | ||||||
| chr8:73995782 | G | A | 151 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.112+4228G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995782 | |||||||
| chr8:73995912 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+4358G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73995912 | |||||||
| chr8:73996017 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.112+4463C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996017 | |||||||
| chr8:73996266 | G | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(66): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.112+4712G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996266 | |||||||
| chr8:73996280 | T | C | 69 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0159 others(66): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.112+4726T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996280 | |||||||
| chr8:73996317 | T | TTTCC | 4 | a0001c0001t0001g0060 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02004.hp2 HG02015.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4811_112+4814d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996317 | ||||||
| chr8:73996317 | T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0171 |
2 | HG03041.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.112+4803_112+4814d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996317 | ||||||
| chr8:73996317 | T | TTTCCTTC others(9): Show |
1 | a0001c0001t0001g0139 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.112+4799_112+4814d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996317 | ||||||
| chr8:73996317 | TTTCCTTC others(1): Show |
T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0061 others(1): Show |
4 | HG01884.hp1 HG03516.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+4807_112+4814d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996317 | ||||||
| chr8:73996317 | TTTCCTTC others(5): Show |
T | 1 | a0004c0003t0003g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112+4803_112+4814d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996317 | ||||||
| chr8:73996329 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.112+4775C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996329 | |||||||
| chr8:73996345 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+4791C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996345 | |||||||
| chr8:73996349 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0002g0035 |
2 | HG02055.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.112+4795C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996349 | |||||||
| chr8:73996353 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+4799C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996353 | |||||||
| chr8:73996353 | CTTCCTTC others(9): Show |
C | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+4806_112+4821d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996353 | ||||||
| chr8:73996356 | CCTTCCTT others(53): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.112+4806_112+4865d others(62): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996356 | ||||||
| chr8:73996357 | C | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0039 others(20): Show |
24 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.112+4803C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996357 | |||||||
| chr8:73996357 | CTTCCTTC others(5): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+4810_112+4821d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996357 | ||||||
| chr8:73996360 | CCTTCCTT others(17): Show |
C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.112+4810_112+4833d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996360 | ||||||
| chr8:73996361 | C | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(51): Show |
56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.112+4807C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996361 | |||||||
| chr8:73996364 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.112+4810C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996364 | |||||||
| chr8:73996364 | CCTTCATT others(5): Show |
C | 3 | a0001c0001t0001g0037 a0004c0003t0003g0012 a0004c0003t0003g0013 |
3 | HG01074.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.112+4814_112+4825d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996364 | ||||||
| chr8:73996364 | CCTTCATT others(9): Show |
C | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112+4814_112+4829d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996364 | ||||||
| chr8:73996364 | CCTTCATT others(33): Show |
C | 1 | a0001c0001t0001g0160 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.112+4814_112+4853d others(42): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996364 | ||||||
| chr8:73996364 | CCTTCATT others(37): Show |
C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+4814_112+4857d others(46): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996364 | ||||||
| chr8:73996364 | CCTTCATT others(45): Show |
C | 7 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+4814_112+4865d others(54): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996364 | ||||||
| chr8:73996365 | C | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(102): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.112+4811C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996365 | |||||||
| chr8:73996365 | CTTCA | C | 3 | a0001c0001t0001g0030 a0001c0001t0002g0024 a0003c0004t0001g0053 |
3 | HG01106.hp2 HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+4815_112+4818d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996365 | ||||||
| chr8:73996368 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0086 a0001c0001t0001g0124 others(1): Show |
4 | HG00099.hp2 HG02280.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4814C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(5): Show |
C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.112+4815_112+4826d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(25): Show |
C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0213 a0001c0001t0001g0232 |
3 | HG00642.hp2 HG03710.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.112+4815_112+4846d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(29): Show |
C | 7 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG00423.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+4815_112+4850d others(38): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(33): Show |
C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0159 a0001c0001t0001g0181 others(32): Show |
36 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.112+4815_112+4854d others(42): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(37): Show |
C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0203 |
2 | HG03225.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.112+4815_112+4858d others(46): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(41): Show |
C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0255 a0001c0001t0001g0256 others(17): Show |
21 | HG00280.hp1 HG00280.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.112+4815_112+4862d others(50): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996368 | CATTCCTT others(45): Show |
C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+4815_112+4866d others(54): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996368 | |||||||
| chr8:73996369 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
88 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.112+4815A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996369 | |||||||
| chr8:73996371 | TC | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0051 others(2): Show |
5 | HG02572.hp2 HG04199.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+4819delC | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996371 | ||||||
| chr8:73996372 | C | CATTCCTT others(1): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0111 a0001c0001t0001g0157 |
3 | HG02738.hp1 HG02965.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.112+4818_112+4819i others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(5): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0073 others(3): Show |
6 | HG00621.hp2 HG02055.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+4818_112+4819i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(9): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0062 others(3): Show |
6 | HG00609.hp1 HG01106.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+4818_112+4819i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(13): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0100 others(1): Show |
4 | HG02040.hp1 NA18942.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+4818_112+4819i others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(17): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0123 others(2): Show |
5 | HG00438.hp2 HG02129.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+4818_112+4819i others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(21): Show |
1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.112+4818_112+4819i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTCCTT others(29): Show |
1 | a0001c0001t0001g0126 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.112+4818_112+4819i others(38): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTTCTT others(5): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0095 |
2 | NA18965.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.112+4818_112+4819i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTTCTT others(9): Show |
6 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0076 others(3): Show |
6 | HG00438.hp1 HG00673.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+4818_112+4819i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CATTTCTT others(17): Show |
1 | a0001c0001t0001g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.112+4818_112+4819i others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | C | CCTTCATT others(5): Show |
4 | a0001c0001t0001g0101 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG00323.hp1 HG00323.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4821_112+4822i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(9): Show |
3 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0002c0002t0001g0120 |
3 | HG01109.hp1 HG02451.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.112+4821_112+4822i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(13): Show |
2 | a0001c0001t0001g0142 a0001c0001t0002g0170 |
2 | HG02109.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.112+4821_112+4822i others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(17): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0151 others(1): Show |
4 | HG02015.hp1 HG02155.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+4821_112+4822i others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(21): Show |
1 | a0001c0001t0001g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(25): Show |
1 | a0001c0001t0001g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(5): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0133 others(1): Show |
5 | HG00558.hp1 HG01515.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+4821_112+4822i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(9): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0141 |
3 | NA18747.hp2 NA19074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.112+4821_112+4822i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCATT others(21): Show |
1 | a0001c0001t0001g0148 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.112+4821_112+4822i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(13): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0164 |
2 | HG02976.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.112+4821_112+4822i others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(17): Show |
1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0001g0105 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(9): Show |
1 | a0001c0001t0001g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(5): Show |
1 | a0001c0001t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+4821_112+4822i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(21): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0179 |
2 | NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.112+4821_112+4822i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(8): Show |
1 | a0001c0001t0001g0016 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.112+4821_112+4822i others(17): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTCCTT others(10): Show |
1 | a0001c0001t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.112+4821_112+4822i others(19): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0045 others(5): Show |
8 | HG00673.hp1 HG01346.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+4883_112+4886d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTTCTT others(1): Show |
7 | a0001c0001t0001g0064 a0001c0001t0001g0099 a0001c0001t0001g0102 others(4): Show |
7 | HG01081.hp1 HG01361.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+4879_112+4886d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTTCTT others(5): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0103 others(3): Show |
6 | HG00639.hp2 HG01993.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+4875_112+4886d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTTCTT others(9): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0114 a0002c0002t0001g0047 others(1): Show |
4 | HG00423.hp1 HG00735.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4871_112+4886d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.112+4867_112+4886d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | CCTTTCTT others(17): Show |
1 | a0001c0001t0001g0048 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.112+4863_112+4886d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0032 others(16): Show |
19 | HG00099.hp2 HG00733.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.112+4818C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996372 | |||||||
| chr8:73996372 | CCTTTCTT others(5): Show |
C | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.112+4875_112+4886d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | CCTTTCTT others(25): Show |
C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0227 |
2 | HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.112+4855_112+4886d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | CCTTTCTT others(29): Show |
C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0196 others(10): Show |
13 | HG00642.hp1 HG01934.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.112+4851_112+4886d others(38): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | CCTTTCTT others(33): Show |
C | 11 | a0001c0001t0001g0163 a0001c0001t0001g0191 a0001c0001t0001g0264 others(8): Show |
11 | HG01243.hp2 HG02080.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+4847_112+4886d others(42): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | CCTTTCTT others(37): Show |
C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
22 | HG00735.hp1 HG01081.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.112+4843_112+4886d others(46): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996372 | CCTTTCTT others(41): Show |
C | 3 | a0001c0001t0001g0021 a0001c0001t0002g0178 a0001c0001t0002g0205 |
3 | HG02922.hp1 HG03098.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.112+4839_112+4886d others(50): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996372 | ||||||
| chr8:73996373 | C | A | 11 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0054 others(8): Show |
11 | HG00558.hp2 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+4819C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996373 | |||||||
| chr8:73996374 | T | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0051 others(2): Show |
5 | HG02572.hp2 HG04199.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+4820T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996374 | |||||||
| chr8:73996374 | T | TTCCTTCC others(11): Show |
1 | a0001c0001t0001g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.112+4821_112+4822i others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73996374 | ||||||
| chr8:73996376 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0054 others(9): Show |
12 | HG00558.hp2 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.112+4822T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996376 | |||||||
| chr8:73996377 | C | A | 1 | a0003c0004t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.112+4823C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996377 | |||||||
| chr8:73996378 | T | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0051 others(3): Show |
6 | HG02572.hp2 HG03471.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+4824T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996378 | |||||||
| chr8:73996380 | T | C | 2 | a0001c0001t0001g0156 a0003c0004t0001g0053 |
2 | HG01106.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.112+4826T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996380 | |||||||
| chr8:73996381 | CTTTCTTT others(24): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.112+4828_112+4858d others(33): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996381 | |||||||
| chr8:73996381 | CTTTCTTT others(32): Show |
C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0051 others(1): Show |
4 | HG04199.hp1 NA18906.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4828_112+4866d others(41): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996381 | |||||||
| chr8:73996382 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+4828T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996382 | |||||||
| chr8:73996384 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112+4830T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996384 | |||||||
| chr8:73996385 | CTTTCTTT others(28): Show |
C | 1 | a0001c0001t0002g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+4832_112+4866d others(37): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996385 | |||||||
| chr8:73996388 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112+4834T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996388 | |||||||
| chr8:73996404 | T | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0213 a0001c0001t0001g0232 |
3 | HG00642.hp2 HG03710.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.112+4850T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996404 | |||||||
| chr8:73996405 | C | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0213 a0001c0001t0001g0232 |
3 | HG00642.hp2 HG03710.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.112+4851C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996405 | |||||||
| chr8:73996408 | T | C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG00642.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+4854T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996408 | |||||||
| chr8:73996409 | C | A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02451.hp2 HG02630.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+4855C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996409 | |||||||
| chr8:73996412 | T | C | 7 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+4858T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996412 | |||||||
| chr8:73996413 | C | A | 11 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(8): Show |
11 | HG02080.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+4859C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996413 | |||||||
| chr8:73996416 | T | C | 11 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(8): Show |
11 | HG02080.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+4862T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996416 | |||||||
| chr8:73996417 | C | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
10 | HG00735.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+4863C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996417 | |||||||
| chr8:73996420 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
10 | HG00735.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+4866T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996420 | |||||||
| chr8:73996547 | A | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.112+4993A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996547 | |||||||
| chr8:73996592 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.112+5038T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996592 | |||||||
| chr8:73996708 | T | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.112+5154T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996708 | |||||||
| chr8:73996758 | T | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG01243.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+5204T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996758 | |||||||
| chr8:73996774 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0062 |
2 | HG00609.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.112+5220T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996774 | |||||||
| chr8:73996784 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+5230G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996784 | |||||||
| chr8:73996905 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112+5351C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996905 | |||||||
| chr8:73996964 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
29 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.112+5410C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73996964 | |||||||
| chr8:73997053 | TTTAG | T | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+5501_112+5504d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73997053 | ||||||
| chr8:73997063 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+5509A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997063 | |||||||
| chr8:73997124 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | HG02055.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+5570C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997124 | |||||||
| chr8:73997312 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112+5758C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997312 | |||||||
| chr8:73997411 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.112+5857G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997411 | |||||||
| chr8:73997501 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+5947T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997501 | |||||||
| chr8:73997562 | A | T | 2 | a0001c0001t0001g0036 a0001c0001t0002g0035 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.112+6008A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997562 | |||||||
| chr8:73997643 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.112+6089C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997643 | |||||||
| chr8:73997902 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
5 | HG00558.hp1 HG02027.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+6348A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997902 | |||||||
| chr8:73997934 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+6380C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997934 | |||||||
| chr8:73997997 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.112+6443C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73997997 | |||||||
| chr8:73998039 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112+6485G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998039 | |||||||
| chr8:73998103 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.112+6549C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998103 | |||||||
| chr8:73998141 | A | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+6587A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998141 | |||||||
| chr8:73998330 | G | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.113-6466G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998330 | |||||||
| chr8:73998347 | C | T | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.113-6449C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998347 | |||||||
| chr8:73998481 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-6315G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998481 | |||||||
| chr8:73998655 | C | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG00735.hp1 HG04199.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-6141C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998655 | |||||||
| chr8:73998691 | C | CA | 67 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0044 others(64): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.113-6097dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73998691 | ||||||
| chr8:73998701 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.113-6095G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998701 | |||||||
| chr8:73998796 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.113-6000A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998796 | |||||||
| chr8:73998874 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.113-5922A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73998874 | |||||||
| chr8:73998975 | A | AT | 146 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.113-5808dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 73998975 | ||||||
| chr8:73999108 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.113-5688C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73999108 | |||||||
| chr8:73999344 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.113-5452C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73999344 | |||||||
| chr8:73999472 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.113-5324C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73999472 | |||||||
| chr8:73999536 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113-5260A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73999536 | |||||||
| chr8:73999799 | A | G | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.113-4997A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 73999799 | |||||||
| chr8:74000006 | C | A | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.113-4790C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000006 | |||||||
| chr8:74000060 | G | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-4736G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000060 | |||||||
| chr8:74000273 | A | AGATAGTG others(12): Show |
49 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0256 others(46): Show |
50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-4518_113-4517i others(21): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74000273 | ||||||
| chr8:74000274 | G | C | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 |
3 | HG01081.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.113-4522G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000274 | |||||||
| chr8:74000279 | A | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.113-4517A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000279 | |||||||
| chr8:74000280 | G | GTAGATCC others(12): Show |
1 | a0001c0001t0001g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.113-4504_113-4503i others(21): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74000280 | ||||||
| chr8:74000484 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.113-4312C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000484 | |||||||
| chr8:74000666 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.113-4130G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74000666 | |||||||
| chr8:74001001 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.113-3795G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001001 | |||||||
| chr8:74001228 | A | AT | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(76): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.113-3553dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001228 | ||||||
| chr8:74001228 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.113-3568A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001228 | |||||||
| chr8:74001228 | AT | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(10): Show |
13 | HG01243.hp2 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-3553delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001228 | ||||||
| chr8:74001285 | G | A | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.113-3511G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001285 | |||||||
| chr8:74001348 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.113-3448C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001348 | |||||||
| chr8:74001412 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-3384G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001412 | |||||||
| chr8:74001605 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.113-3191A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001605 | |||||||
| chr8:74001652 | G | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.113-3144G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001652 | |||||||
| chr8:74001688 | C | CA | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG00735.hp1 HG02738.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-3097dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001688 | ||||||
| chr8:74001817 | G | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-2979G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001817 | |||||||
| chr8:74001937 | A | ACCTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
10 | HG01069.hp2 HG01106.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2820_113-2817d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001937 | ||||||
| chr8:74001937 | A | ACCTTCCT others(5): Show |
1 | a0003c0004t0001g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113-2828_113-2817d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001937 | ||||||
| chr8:74001937 | ACCTT | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(56): Show |
62 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.113-2820_113-2817d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001937 | ||||||
| chr8:74001937 | ACCTTCCT others(1): Show |
A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0037 others(28): Show |
32 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.113-2824_113-2817d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001937 | ||||||
| chr8:74001937 | ACCTTCCT others(5): Show |
A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
31 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.113-2828_113-2817d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001937 | ||||||
| chr8:74001968 | T | C | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0002g0006 others(3): Show |
7 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-2828T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001968 | |||||||
| chr8:74001972 | T | C | 41 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0163 others(38): Show |
42 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2824T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001972 | |||||||
| chr8:74001975 | C | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(11): Show |
14 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-2821C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001975 | |||||||
| chr8:74001976 | T | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0133 a0001c0001t0001g0159 others(51): Show |
56 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.113-2820T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001976 | |||||||
| chr8:74001976 | TTCCCTCC others(9): Show |
T | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113-2816_113-2801d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001976 | ||||||
| chr8:74001980 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(55): Show |
61 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-2816C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001980 | |||||||
| chr8:74001984 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0057 others(18): Show |
23 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.113-2812C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001984 | |||||||
| chr8:74001986 | C | T | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0002g0006 others(3): Show |
7 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-2810C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001986 | |||||||
| chr8:74001988 | C | T | 35 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0185 others(32): Show |
36 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.113-2808C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001988 | |||||||
| chr8:74001988 | CTCCCTCC others(5): Show |
C | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG00280.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.113-2804_113-2793d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001988 | ||||||
| chr8:74001988 | CTCCCTCC others(17): Show |
C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01255.hp2 HG01261.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.113-2804_113-2781d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001988 | ||||||
| chr8:74001988 | CTCCCTCC others(21): Show |
C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG01081.hp2 HG01255.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.113-2804_113-2777d others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001988 | ||||||
| chr8:74001988 | CTCCCTCC others(25): Show |
C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0276 |
3 | HG01515.hp1 HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.113-2804_113-2773d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001988 | ||||||
| chr8:74001988 | CTCCCTCC others(29): Show |
C | 4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2804_113-2769d others(38): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001988 | ||||||
| chr8:74001990 | C | T | 27 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0185 others(24): Show |
27 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.113-2806C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001990 | |||||||
| chr8:74001992 | C | T | 41 | a0001c0001t0001g0044 a0001c0001t0001g0133 a0001c0001t0001g0159 others(38): Show |
42 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2804C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001992 | |||||||
| chr8:74001992 | CTCCTTTC others(1): Show |
C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(2): Show |
5 | HG00735.hp1 HG01981.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2790_113-2783d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001992 | ||||||
| chr8:74001992 | CTCCTTTC others(9): Show |
C | 5 | a0001c0001t0001g0128 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG00735.hp2 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2798_113-2783d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001992 | ||||||
| chr8:74001992 | CTCCTTTC others(13): Show |
C | 2 | a0001c0001t0001g0267 a0001c0001t0002g0299 |
2 | HG02922.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.113-2798_113-2779d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001992 | ||||||
| chr8:74001992 | CTCCTTTC others(17): Show |
C | 1 | a0001c0001t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.113-2798_113-2775d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001992 | ||||||
| chr8:74001992 | CTCCTTTC others(21): Show |
C | 2 | a0001c0001t0001g0266 a0001c0001t0002g0265 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.113-2798_113-2771d others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001992 | ||||||
| chr8:74001994 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0133 a0001c0001t0001g0183 others(7): Show |
10 | HG00408.hp2 HG01109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2802C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001994 | |||||||
| chr8:74001994 | CCTTT | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0048 others(24): Show |
29 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-2798_113-2795d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001994 | ||||||
| chr8:74001994 | CCTTTCTT others(5): Show |
C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01952.hp2 HG01993.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2798_113-2787d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001994 | ||||||
| chr8:74001996 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
17 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.113-2800T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001996 | |||||||
| chr8:74001996 | T | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0174 others(1): Show |
5 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2800T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001996 | |||||||
| chr8:74001998 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0056 others(26): Show |
31 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.113-2798T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74001998 | |||||||
| chr8:74001998 | TCTTCCTT others(5): Show |
T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0257 a0001c0001t0001g0297 |
3 | HG02040.hp2 HG02148.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.113-2790_113-2779d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001998 | ||||||
| chr8:74001998 | TCTTCCTT others(9): Show |
T | 6 | a0001c0001t0001g0258 a0001c0001t0001g0263 a0001c0001t0001g0290 others(3): Show |
6 | HG01256.hp2 HG01361.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-2790_113-2775d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001998 | ||||||
| chr8:74001998 | TCTTCCTT others(13): Show |
T | 8 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0259 others(5): Show |
8 | HG01258.hp2 HG01978.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-2790_113-2771d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001998 | ||||||
| chr8:74001998 | TCTTCCTT others(17): Show |
T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0294 a0001c0001t0001g0296 |
3 | HG01975.hp2 HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.113-2790_113-2767d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001998 | ||||||
| chr8:74001998 | TCTTCCTT others(33): Show |
T | 1 | a0001c0001t0001g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.113-2790_113-2751d others(42): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74001998 | ||||||
| chr8:74002000 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(38): Show |
44 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.113-2796T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002000 | |||||||
| chr8:74002000 | T | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0205 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.113-2796T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002000 | |||||||
| chr8:74002002 | C | T | 38 | a0001c0001t0001g0044 a0001c0001t0001g0129 a0001c0001t0001g0133 others(35): Show |
39 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-2794C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002002 | |||||||
| chr8:74002002 | CCTTT | C | 6 | a0001c0001t0001g0244 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-2790_113-2787d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002002 | ||||||
| chr8:74002006 | T | C | 43 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.113-2790T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002006 | |||||||
| chr8:74002006 | TCTTC | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0264 a0001c0001t0002g0014 |
3 | HG02895.hp1 HG03579.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.113-2722_113-2719d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(1): Show |
T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0065 a0001c0001t0001g0067 others(12): Show |
15 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-2726_113-2719d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(5): Show |
T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
20 | HG00609.hp2 HG01074.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.113-2730_113-2719d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(9): Show |
T | 10 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0099 others(7): Show |
10 | HG01361.hp2 HG01952.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-2734_113-2719d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(13): Show |
T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01884.hp1 HG01978.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2738_113-2719d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(17): Show |
T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.113-2742_113-2719d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(21): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.113-2746_113-2719d others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(25): Show |
T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0186 |
2 | HG00438.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.113-2750_113-2719d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002006 | TCTTCCTT others(29): Show |
T | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.113-2754_113-2719d others(38): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002006 | ||||||
| chr8:74002008 | T | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01952.hp2 HG01993.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-2788T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002008 | |||||||
| chr8:74002008 | T | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-2788T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002008 | |||||||
| chr8:74002010 | C | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0129 others(37): Show |
43 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.113-2786C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002010 | |||||||
| chr8:74002012 | T | C | 6 | a0001c0001t0001g0128 a0001c0001t0001g0189 a0001c0001t0001g0268 others(3): Show |
6 | HG00735.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-2784T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002012 | |||||||
| chr8:74002012 | T | G | 6 | a0001c0001t0001g0244 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-2784T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002012 | |||||||
| chr8:74002014 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(47): Show |
54 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.113-2782C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002014 | |||||||
| chr8:74002016 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0267 a0001c0001t0002g0299 |
3 | HG02922.hp2 HG03209.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.113-2780T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002016 | |||||||
| chr8:74002016 | T | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(9): Show |
12 | HG00280.hp1 HG00735.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-2780T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002016 | |||||||
| chr8:74002018 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
29 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-2778C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002018 | |||||||
| chr8:74002020 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0270 |
2 | HG00280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.113-2776T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002020 | |||||||
| chr8:74002020 | T | G | 4 | a0001c0001t0001g0228 a0001c0001t0001g0257 a0001c0001t0001g0264 others(1): Show |
4 | HG02040.hp2 HG02148.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2776T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002020 | |||||||
| chr8:74002022 | C | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(35): Show |
40 | HG00280.hp1 HG00733.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.113-2774C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002022 | |||||||
| chr8:74002024 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0002g0265 |
3 | HG00280.hp2 HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.113-2772T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002024 | |||||||
| chr8:74002024 | T | G | 7 | a0001c0001t0001g0258 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | HG01256.hp2 HG01361.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-2772T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002024 | |||||||
| chr8:74002026 | C | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(40): Show |
46 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.113-2770C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002026 | |||||||
| chr8:74002028 | T | G | 13 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0259 others(10): Show |
13 | HG01255.hp2 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-2768T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002028 | |||||||
| chr8:74002030 | C | T | 54 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.113-2766C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002030 | |||||||
| chr8:74002032 | T | G | 9 | a0001c0001t0001g0261 a0001c0001t0001g0267 a0001c0001t0001g0282 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.113-2764T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002032 | |||||||
| chr8:74002034 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
63 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.113-2762C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002034 | |||||||
| chr8:74002036 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0276 |
4 | HG01515.hp1 HG02602.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2760T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002036 | |||||||
| chr8:74002038 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.113-2755_113-2754i others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002038 | ||||||
| chr8:74002038 | C | T | 72 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
74 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.113-2758C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002038 | |||||||
| chr8:74002040 | T | G | 7 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0278 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-2756T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002040 | |||||||
| chr8:74002042 | C | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.113-2754C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002042 | |||||||
| chr8:74002046 | C | CCTTTCTT others(5): Show |
1 | a0001c0001t0001g0303 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.113-2747_113-2746i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002046 | ||||||
| chr8:74002046 | C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.113-2747_113-2746i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002046 | ||||||
| chr8:74002046 | C | T | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(97): Show |
103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.113-2750C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002046 | |||||||
| chr8:74002046 | CCTTCCTT others(25): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.113-2746_113-2715d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002046 | ||||||
| chr8:74002047 | C | T | 1 | a0004c0003t0003g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113-2749C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002047 | |||||||
| chr8:74002048 | T | G | 1 | a0001c0001t0001g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.113-2748T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002048 | |||||||
| chr8:74002050 | C | CCTTTCTT others(5): Show |
1 | a0001c0001t0001g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.113-2743_113-2742i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002050 | ||||||
| chr8:74002050 | C | CCTTTCTT others(9): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0238 |
2 | HG01934.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.113-2743_113-2742i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002050 | ||||||
| chr8:74002050 | C | T | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(114): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.113-2746C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002050 | |||||||
| chr8:74002054 | C | T | 130 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(127): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.113-2742C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002054 | |||||||
| chr8:74002054 | CCTTCCTT others(17): Show |
C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0034 others(2): Show |
5 | HG02055.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2738_113-2715d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002054 | ||||||
| chr8:74002054 | CCTTCCTT others(21): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.113-2738_113-2711d others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002054 | ||||||
| chr8:74002055 | C | T | 2 | a0004c0003t0003g0012 a0004c0003t0003g0013 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.113-2741C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002055 | |||||||
| chr8:74002058 | C | CCTTTCTT others(21): Show |
1 | a0001c0001t0001g0231 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.113-2735_113-2734i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002058 | ||||||
| chr8:74002058 | C | T | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(138): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.113-2738C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002058 | |||||||
| chr8:74002058 | CCTTCCTT others(13): Show |
C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0002g0026 others(1): Show |
4 | HG01081.hp1 HG02027.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2734_113-2715d others(22): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002058 | ||||||
| chr8:74002058 | CCTTCCTT others(17): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113-2734_113-2711d others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002058 | ||||||
| chr8:74002058 | CCTTCCTT others(21): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.113-2734_113-2707d others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002058 | ||||||
| chr8:74002058 | CCTTCCTT others(25): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113-2734_113-2703d others(34): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002058 | ||||||
| chr8:74002061 | TCCTTCCT others(27): Show |
T | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-2734_113-2701d others(36): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002061 | |||||||
| chr8:74002062 | C | T | 148 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(145): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.113-2734C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002062 | |||||||
| chr8:74002062 | CCTTCCTT others(9): Show |
C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0146 a0001c0001t0002g0025 others(1): Show |
4 | HG00423.hp1 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2730_113-2715d others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002062 | ||||||
| chr8:74002065 | TCCTTCCT others(7): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113-2730_113-2717d others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002065 | |||||||
| chr8:74002066 | C | T | 151 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(148): Show |
155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.113-2730C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002066 | |||||||
| chr8:74002066 | CCTTCCTT others(5): Show |
C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0140 a0002c0002t0001g0047 |
3 | HG02698.hp1 HG03654.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.113-2726_113-2715d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002066 | ||||||
| chr8:74002070 | C | T | 161 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.113-2726C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002070 | |||||||
| chr8:74002070 | CCTTCCTT others(1): Show |
C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0002g0024 others(1): Show |
4 | HG00621.hp2 HG02055.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2722_113-2715d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002070 | ||||||
| chr8:74002073 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0174 |
3 | HG02615.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.113-2723T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002073 | |||||||
| chr8:74002074 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(183): Show |
192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.113-2722C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002074 | |||||||
| chr8:74002077 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0180 others(1): Show |
4 | HG01167.hp2 HG01884.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2719T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002077 | |||||||
| chr8:74002078 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0055 others(8): Show |
13 | HG00323.hp1 HG01106.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-2718T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002078 | |||||||
| chr8:74002079 | CTT | C | 3 | a0001c0001t0001g0030 a0001c0001t0002g0006 a0001c0001t0002g0174 |
3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.113-2715_113-2714d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002079 | ||||||
| chr8:74002081 | T | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(8): Show |
11 | HG01074.hp1 HG01167.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.113-2715T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002081 | |||||||
| chr8:74002083 | C | CTTTCTTT others(37): Show |
1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(46): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002083 | ||||||
| chr8:74002085 | T | C | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
15 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-2711T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002085 | |||||||
| chr8:74002085 | TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0001g0004 | 2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.113-2707_113-2698d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002085 | ||||||
| chr8:74002085 | TTCTTTCT others(7): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-2707_113-2694d others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002085 | ||||||
| chr8:74002087 | CTT | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0027 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2707_113-2706d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002087 | ||||||
| chr8:74002089 | T | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(16): Show |
20 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.113-2707T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002089 | |||||||
| chr8:74002089 | TTCTTTCT others(3): Show |
T | 14 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0071 others(11): Show |
14 | HG02129.hp1 HG02155.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-2703_113-2694d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002089 | ||||||
| chr8:74002089 | TTCTTTCT others(5): Show |
T | 2 | a0001c0001t0001g0048 a0003c0004t0001g0059 |
2 | HG00639.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.113-2703_113-2692d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002089 | ||||||
| chr8:74002089 | TTCTTTCT others(7): Show |
T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0116 a0001c0001t0001g0272 others(2): Show |
5 | HG00558.hp2 HG02080.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2703_113-2690d others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002089 | ||||||
| chr8:74002089 | TTCTTTCT others(11): Show |
T | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.113-2703_113-2686d others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002089 | ||||||
| chr8:74002091 | CTT | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0223 a0001c0001t0001g0248 others(1): Show |
4 | HG01069.hp2 HG01934.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2703_113-2702d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002091 | ||||||
| chr8:74002092 | TTTCTCTC others(4): Show |
T | 1 | a0001c0001t0001g0273 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.113-2702_113-2692d others(13): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002092 | ||||||
| chr8:74002093 | T | C | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(39): Show |
43 | HG00642.hp1 HG01069.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.113-2703T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002093 | |||||||
| chr8:74002093 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0204 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.113-2673_113-2664d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113-2675_113-2664d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTCTC others(4): Show |
1 | a0001c0001t0001g0235 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(13): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(5): Show |
1 | a0001c0001t0001g0220 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0217 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(24): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(3): Show |
4 | a0001c0001t0001g0185 a0001c0001t0001g0226 a0001c0001t0001g0229 others(1): Show |
4 | HG00741.hp2 HG01496.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2700_113-2699i others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(17): Show |
1 | a0001c0001t0001g0200 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(26): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(6): Show |
1 | a0001c0001t0001g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(15): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(8): Show |
1 | a0001c0001t0001g0246 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(17): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(18): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(11): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0001g0241 |
3 | HG02257.hp2 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.113-2700_113-2699i others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(21): Show |
1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0192 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(24): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(21): Show |
1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0002g0008 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(36): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(32): Show |
1 | a0001c0001t0002g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(41): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(36): Show |
1 | a0001c0001t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(45): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(21): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0181 a0001c0001t0001g0230 |
4 | HG01099.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2700_113-2699i others(30): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.113-2700_113-2699i others(36): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTC | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(56): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.113-2665_113-2664d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTC | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0107 others(5): Show |
8 | HG00609.hp1 HG02015.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-2667_113-2664d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTCTC | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0045 others(39): Show |
42 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2669_113-2664d others(8): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTCTCT others(1): Show |
T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0125 others(1): Show |
4 | HG00609.hp2 HG01106.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2671_113-2664d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTCTCT others(3): Show |
T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0103 others(4): Show |
7 | HG00280.hp1 HG01256.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-2673_113-2664d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.113-2675_113-2664d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002093 | TTCTCTCT others(7): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0129 |
3 | HG00673.hp1 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.113-2677_113-2664d others(16): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002093 | ||||||
| chr8:74002095 | C | CTTTATTT others(11): Show |
1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-2700_113-2699i others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002095 | ||||||
| chr8:74002095 | C | CTTTCTTT others(11): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0211 |
2 | HG00423.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.113-2700_113-2699i others(20): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002095 | ||||||
| chr8:74002095 | C | CTTTCTTT others(15): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0198 a0001c0001t0001g0242 |
3 | HG02258.hp2 HG03453.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.113-2700_113-2699i others(24): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002095 | ||||||
| chr8:74002097 | C | CTCTT | 2 | a0001c0001t0001g0009 a0001c0001t0001g0251 |
3 | HG00733.hp1 HG01175.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.113-2696_113-2695i others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002097 | ||||||
| chr8:74002097 | C | T | 45 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0074 others(42): Show |
45 | HG00423.hp1 HG00621.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.113-2699C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002097 | |||||||
| chr8:74002099 | C | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0015 others(53): Show |
58 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.113-2697C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002099 | |||||||
| chr8:74002100 | TC | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0269 a0001c0001t0001g0297 |
3 | HG01981.hp1 HG02109.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.113-2695delC | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002100 | |||||||
| chr8:74002101 | C | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0085 others(18): Show |
22 | HG00733.hp1 HG01109.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.113-2695C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002101 | |||||||
| chr8:74002103 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0099 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.113-2693C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002103 | |||||||
| chr8:74002105 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0254 |
2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.113-2691C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002105 | |||||||
| chr8:74002107 | C | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
10 | HG00735.hp1 HG02572.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2689C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002107 | |||||||
| chr8:74002111 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.113-2685C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002111 | |||||||
| chr8:74002131 | CT | C | 5 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0262 others(2): Show |
5 | HG01256.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2662delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002131 | ||||||
| chr8:74002132 | T | TC | 8 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0192 others(5): Show |
8 | HG01496.hp1 HG03130.hp2 NA19001.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-2664_113-2663i others(3): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002132 | |||||||
| chr8:74002272 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.113-2524G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002272 | |||||||
| chr8:74002458 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG00735.hp1 HG04199.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-2338C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002458 | |||||||
| chr8:74002556 | G | T | 9 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(6): Show |
10 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-2240G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002556 | |||||||
| chr8:74002569 | A | C | 4 | a0001c0001t0001g0168 a0001c0001t0001g0222 a0001c0001t0001g0240 others(1): Show |
4 | HG00621.hp1 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2227A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002569 | |||||||
| chr8:74002573 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.113-2223C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002573 | |||||||
| chr8:74002573 | C | CT | 9 | a0001c0001t0001g0182 a0001c0001t0001g0198 a0001c0001t0001g0211 others(6): Show |
9 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.113-2207dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002573 | ||||||
| chr8:74002573 | CT | C | 13 | a0001c0001t0001g0038 a0001c0001t0001g0076 a0001c0001t0001g0119 others(10): Show |
13 | HG00621.hp2 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-2207delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002573 | ||||||
| chr8:74002573 | CTT | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(16): Show |
21 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.113-2208_113-2207d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002573 | ||||||
| chr8:74002657 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(4): Show |
7 | HG01074.hp1 HG01167.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-2139C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002657 | |||||||
| chr8:74002746 | A | AT | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-2043dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74002746 | ||||||
| chr8:74002799 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.113-1997C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002799 | |||||||
| chr8:74002816 | T | C | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(79): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.113-1980T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002816 | |||||||
| chr8:74002864 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-1932G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74002864 | |||||||
| chr8:74003202 | CAGG | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.113-1589_113-1587d others(5): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 74003202 | ||||||
| chr8:74003434 | T | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.113-1362T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003434 | |||||||
| chr8:74003470 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113-1326T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003470 | |||||||
| chr8:74003534 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.113-1262C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003534 | |||||||
| chr8:74003535 | G | A | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1261G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003535 | |||||||
| chr8:74003686 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.113-1110G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003686 | |||||||
| chr8:74003699 | A | G | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-1097A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003699 | |||||||
| chr8:74003779 | C | T | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.113-1017C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003779 | |||||||
| chr8:74003922 | C | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0138 others(2): Show |
5 | HG00673.hp2 NA18947.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-874C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74003922 | |||||||
| chr8:74004109 | C | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-687C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004109 | |||||||
| chr8:74004111 | G | T | 8 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0173 others(5): Show |
9 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.113-685G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004111 | |||||||
| chr8:74004482 | A | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.113-314A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004482 | |||||||
| chr8:74004492 | A | G | 6 | a0001c0001t0001g0206 a0001c0001t0001g0219 a0001c0001t0001g0225 others(3): Show |
6 | HG00408.hp2 HG00621.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-304A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004492 | |||||||
| chr8:74004655 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.113-141G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004655 | |||||||
| chr8:74004706 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.113-90A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 1/4 | chr8 | 74004706 | |||||||
| chr8:74004917 | T | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+32T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74004917 | |||||||
| chr8:74004974 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.202+89C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74004974 | |||||||
| chr8:74004993 | A | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0189 a0001c0001t0001g0255 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.202+108A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74004993 | |||||||
| chr8:74005120 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.202+235G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005120 | |||||||
| chr8:74005149 | G | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0277 a0001c0001t0001g0281 others(5): Show |
9 | HG00280.hp1 HG01255.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+264G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005149 | |||||||
| chr8:74005397 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.202+512C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005397 | |||||||
| chr8:74005786 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.202+901C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005786 | |||||||
| chr8:74005801 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.202+916G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005801 | |||||||
| chr8:74005936 | G | A | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.202+1051G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005936 | |||||||
| chr8:74005960 | G | A | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1075G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005960 | |||||||
| chr8:74005968 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0078 |
2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.202+1083T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74005968 | |||||||
| chr8:74006160 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.202+1275G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006160 | |||||||
| chr8:74006343 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.202+1458A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006343 | |||||||
| chr8:74006467 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.202+1582G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006467 | |||||||
| chr8:74006487 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1602C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006487 | |||||||
| chr8:74006509 | C | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+1624C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006509 | |||||||
| chr8:74006636 | T | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(82): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+1751T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006636 | |||||||
| chr8:74006643 | C | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0212 a0001c0001t0001g0228 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+1758C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006643 | |||||||
| chr8:74006822 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG01243.hp2 HG01993.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+1937C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006822 | |||||||
| chr8:74006938 | A | G | 2 | a0003c0004t0001g0053 a0003c0004t0001g0059 |
2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.202+2053A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74006938 | |||||||
| chr8:74007050 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.202+2165T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007050 | |||||||
| chr8:74007062 | C | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG01109.hp2 HG06807.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+2177C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007062 | |||||||
| chr8:74007077 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.202+2192C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007077 | |||||||
| chr8:74007094 | G | C | 136 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(133): Show |
140 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.202+2209G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007094 | |||||||
| chr8:74007140 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.202+2255A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007140 | |||||||
| chr8:74007142 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.202+2257C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007142 | |||||||
| chr8:74007144 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.202+2259A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007144 | |||||||
| chr8:74007150 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.202+2265G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007150 | |||||||
| chr8:74007151 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.202+2266G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007151 | |||||||
| chr8:74007245 | G | A | 22 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0030 others(19): Show |
22 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.202+2360G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007245 | |||||||
| chr8:74007461 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.203-2540A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007461 | |||||||
| chr8:74007478 | T | C | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(101): Show |
108 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.203-2523T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007478 | |||||||
| chr8:74007483 | G | C | 3 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0147 |
3 | HG02055.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.203-2518G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007483 | |||||||
| chr8:74007514 | A | T | 94 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
96 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.203-2487A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007514 | |||||||
| chr8:74007528 | A | G | 94 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
96 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.203-2473A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007528 | |||||||
| chr8:74007677 | T | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0063 others(29): Show |
33 | HG00621.hp2 HG00733.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.203-2324T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007677 | |||||||
| chr8:74007715 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.203-2286G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007715 | |||||||
| chr8:74007770 | C | T | 34 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(31): Show |
36 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.203-2231C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007770 | |||||||
| chr8:74007806 | C | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-2195C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007806 | |||||||
| chr8:74007828 | C | T | 34 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(31): Show |
36 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.203-2173C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007828 | |||||||
| chr8:74007831 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-2170C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007831 | |||||||
| chr8:74007904 | C | T | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.203-2097C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007904 | |||||||
| chr8:74007975 | G | C | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG02976.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-2026G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74007975 | |||||||
| chr8:74008007 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.203-1994G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008007 | |||||||
| chr8:74008039 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-1962C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008039 | |||||||
| chr8:74008103 | A | G | 131 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(128): Show |
134 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.203-1898A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008103 | |||||||
| chr8:74008339 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.203-1662C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008339 | |||||||
| chr8:74008363 | A | G | 133 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(130): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.203-1638A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008363 | |||||||
| chr8:74008426 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0102 a0001c0001t0001g0292 |
3 | HG02080.hp1 NA18944.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.203-1575A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008426 | |||||||
| chr8:74008572 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.203-1429G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008572 | |||||||
| chr8:74008619 | G | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-1382G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008619 | |||||||
| chr8:74008620 | AAT | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-1380_203-1379d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008620 | |||||||
| chr8:74008623 | T | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-1378T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008623 | |||||||
| chr8:74008625 | T | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-1376T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008625 | |||||||
| chr8:74008858 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.203-1143C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008858 | |||||||
| chr8:74008938 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.203-1063G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008938 | |||||||
| chr8:74008991 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0134 |
3 | HG00558.hp1 HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.203-1010G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74008991 | |||||||
| chr8:74009186 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.203-815G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74009186 | |||||||
| chr8:74009374 | C | CA | 24 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0081 others(21): Show |
24 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.203-602dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009374 | ||||||
| chr8:74009374 | CA | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(86): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.203-602delA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009374 | ||||||
| chr8:74009374 | CAA | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(12): Show |
15 | HG01069.hp1 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-603_203-602del others(2): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009374 | ||||||
| chr8:74009374 | CAAAA | C | 8 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(5): Show |
10 | HG02145.hp2 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.203-605_203-602del others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009374 | ||||||
| chr8:74009395 | A | AAAGAAG | 6 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-604_203-603ins others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009395 | ||||||
| chr8:74009397 | A | G | 10 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0034 others(7): Show |
10 | HG01081.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-604A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74009397 | |||||||
| chr8:74009400 | G | GAA | 6 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-600_203-599dup others(2): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009400 | ||||||
| chr8:74009400 | G | GAAAAGAA | 10 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0034 others(7): Show |
10 | HG01081.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-599_203-598ins others(7): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 74009400 | ||||||
| chr8:74009405 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.203-596A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 2/4 | chr8 | 74009405 | |||||||
| chr8:74010200 | A | G | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.331+71A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74010200 | |||||||
| chr8:74010504 | T | TA | 7 | a0001c0001t0001g0212 a0001c0001t0001g0228 a0001c0001t0001g0244 others(4): Show |
7 | HG01346.hp1 HG01981.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+383dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74010504 | ||||||
| chr8:74010769 | T | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0228 a0001c0001t0001g0244 others(5): Show |
8 | HG01346.hp1 HG01981.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+640T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74010769 | |||||||
| chr8:74010880 | GA | G | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.331+761delA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74010880 | ||||||
| chr8:74010908 | GT | G | 129 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(126): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.331+790delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74010908 | ||||||
| chr8:74011099 | T | A | 3 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0147 |
3 | HG02055.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.331+970T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011099 | |||||||
| chr8:74011102 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+973T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011102 | |||||||
| chr8:74011107 | G | A | 42 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(39): Show |
44 | HG01081.hp1 HG01346.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.331+978G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011107 | |||||||
| chr8:74011110 | C | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 |
3 | HG01081.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.331+981C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011110 | |||||||
| chr8:74011421 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331+1292G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011421 | |||||||
| chr8:74011432 | C | T | 67 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.331+1303C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011432 | |||||||
| chr8:74011480 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.331+1351T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011480 | |||||||
| chr8:74011509 | T | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(90): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.331+1380T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011509 | |||||||
| chr8:74011587 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.331+1458G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011587 | |||||||
| chr8:74011598 | C | T | 13 | a0001c0001t0001g0141 a0001c0001t0002g0006 a0001c0001t0002g0008 others(10): Show |
15 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.331+1469C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011598 | |||||||
| chr8:74011599 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.331+1470G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011599 | |||||||
| chr8:74011646 | G | A | 93 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(90): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.331+1517G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011646 | |||||||
| chr8:74011782 | C | A | 7 | a0001c0001t0001g0066 a0001c0001t0001g0100 a0001c0001t0001g0102 others(4): Show |
7 | HG02080.hp1 NA18944.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+1653C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011782 | |||||||
| chr8:74011807 | C | T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0164 a0001c0001t0001g0166 others(4): Show |
7 | HG00323.hp2 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+1678C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74011807 | |||||||
| chr8:74011858 | C | CA | 27 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0079 others(24): Show |
27 | HG00438.hp1 HG00621.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.331+1748dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74011858 | ||||||
| chr8:74011858 | CA | C | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
44 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.331+1748delA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74011858 | ||||||
| chr8:74011951 | T | TAAAACAT others(10): Show |
130 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(127): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.331+1823_331+1824i others(19): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74011951 | ||||||
| chr8:74012069 | A | G | 34 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(31): Show |
36 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.331+1940A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012069 | |||||||
| chr8:74012082 | T | C | 34 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(31): Show |
36 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.331+1953T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012082 | |||||||
| chr8:74012217 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.331+2088A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012217 | |||||||
| chr8:74012675 | A | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0054 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.331+2546A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012675 | |||||||
| chr8:74012776 | T | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.331+2647T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012776 | |||||||
| chr8:74012779 | C | G | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+2650C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012779 | |||||||
| chr8:74012875 | A | G | 3 | a0004c0003t0003g0011 a0004c0003t0003g0012 a0004c0003t0003g0013 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.331+2746A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012875 | |||||||
| chr8:74012918 | A | G | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.331+2789A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74012918 | |||||||
| chr8:74013172 | T | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(127): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.331+3043T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013172 | |||||||
| chr8:74013219 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331+3090G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013219 | |||||||
| chr8:74013381 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.331+3252C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013381 | |||||||
| chr8:74013384 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.331+3255A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013384 | |||||||
| chr8:74013482 | C | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(90): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.331+3353C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013482 | |||||||
| chr8:74013608 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.331+3479G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013608 | |||||||
| chr8:74013961 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.331+3832A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74013961 | |||||||
| chr8:74014085 | A | AT | 26 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.331+3961dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014085 | ||||||
| chr8:74014250 | G | GA | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
47 | HG01081.hp1 HG01346.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.331+4135dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014250 | ||||||
| chr8:74014269 | C | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+4140C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014269 | |||||||
| chr8:74014394 | GA | G | 81 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(78): Show |
82 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.331+4277delA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014394 | ||||||
| chr8:74014395 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.331+4266A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014395 | |||||||
| chr8:74014395 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0196 |
2 | HG01975.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.331+4266A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014395 | |||||||
| chr8:74014484 | G | GT | 24 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
24 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.331+4374dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014484 | ||||||
| chr8:74014484 | GT | G | 78 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0038 others(75): Show |
79 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.331+4374delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014484 | ||||||
| chr8:74014574 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0203 a0001c0001t0001g0271 |
3 | HG01243.hp2 HG03225.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.331+4445A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014574 | |||||||
| chr8:74014639 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331+4510C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014639 | |||||||
| chr8:74014667 | G | C | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+4538G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014667 | |||||||
| chr8:74014670 | G | A | 26 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(23): Show |
28 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.331+4541G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014670 | |||||||
| chr8:74014812 | T | TAC | 143 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0028 others(140): Show |
145 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.331+4717_331+4718d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | T | TACAC | 36 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(33): Show |
36 | HG00408.hp2 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.331+4715_331+4718d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | T | TACACAC | 7 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0219 others(4): Show |
8 | HG02155.hp2 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+4713_331+4718d others(8): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0002g0014 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+4711_331+4718d others(10): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | T | TACACACA others(3): Show |
5 | a0001c0001t0002g0023 a0001c0001t0002g0172 a0001c0001t0002g0175 others(2): Show |
5 | HG02622.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+4709_331+4718d others(12): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | T | TACACACA others(5): Show |
3 | a0001c0001t0002g0006 a0001c0001t0002g0174 a0001c0001t0002g0176 |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+4707_331+4718d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | TAC | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0202 a0001c0001t0001g0298 others(1): Show |
4 | HG00438.hp2 HG01934.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+4717_331+4718d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | TACAC | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0117 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG03927.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.331+4715_331+4718d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014812 | TACACACA others(5): Show |
T | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.331+4707_331+4718d others(14): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74014812 | ||||||
| chr8:74014848 | T | C | 66 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(63): Show |
67 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+4719T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014848 | |||||||
| chr8:74014951 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+4822A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74014951 | |||||||
| chr8:74015036 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.331+4907G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015036 | |||||||
| chr8:74015155 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+5026C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015155 | |||||||
| chr8:74015156 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331+5027G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015156 | |||||||
| chr8:74015309 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.331+5180A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015309 | |||||||
| chr8:74015413 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.331+5284T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015413 | |||||||
| chr8:74015558 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+5429C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015558 | |||||||
| chr8:74015630 | T | G | 1 | a0001c0001t0001g0294 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.331+5501T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015630 | |||||||
| chr8:74015697 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.331+5568A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015697 | |||||||
| chr8:74015709 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.331+5580C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015709 | |||||||
| chr8:74015833 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.331+5704C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015833 | |||||||
| chr8:74015857 | C | T | 98 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+5728C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015857 | |||||||
| chr8:74015865 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.331+5736C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015865 | |||||||
| chr8:74015891 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+5762C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015891 | |||||||
| chr8:74015904 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+5775C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015904 | |||||||
| chr8:74015939 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+5810G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74015939 | |||||||
| chr8:74016068 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+5939C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016068 | |||||||
| chr8:74016214 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+6085T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016214 | |||||||
| chr8:74016318 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0302 |
2 | NA18941.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.331+6189C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016318 | |||||||
| chr8:74016380 | C | G | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG02976.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+6251C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016380 | |||||||
| chr8:74016418 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0069 |
3 | HG00609.hp2 NA18942.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.331+6289C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016418 | |||||||
| chr8:74016519 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331+6390A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016519 | |||||||
| chr8:74016594 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0279 a0001c0001t0001g0284 |
3 | HG01433.hp1 HG01515.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.331+6465G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016594 | |||||||
| chr8:74016888 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.331+6759C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74016888 | |||||||
| chr8:74017020 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02451.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.331+6891A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017020 | |||||||
| chr8:74017026 | G | A | 3 | a0004c0003t0003g0011 a0004c0003t0003g0012 a0004c0003t0003g0013 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.331+6897G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017026 | |||||||
| chr8:74017091 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.331+6962T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017091 | |||||||
| chr8:74017159 | G | C | 98 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+7030G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017159 | |||||||
| chr8:74017334 | A | G | 114 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(111): Show |
117 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.331+7205A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017334 | |||||||
| chr8:74017379 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+7250G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017379 | |||||||
| chr8:74017398 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.331+7269C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017398 | |||||||
| chr8:74017569 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.331+7440C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017569 | |||||||
| chr8:74017590 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.331+7461A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017590 | |||||||
| chr8:74017684 | C | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(82): Show |
86 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.331+7555C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017684 | |||||||
| chr8:74017760 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+7631G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017760 | |||||||
| chr8:74017762 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+7633C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017762 | |||||||
| chr8:74017763 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.331+7634A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017763 | |||||||
| chr8:74017870 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(25): Show |
30 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+7741C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017870 | |||||||
| chr8:74017904 | C | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+7775C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017904 | |||||||
| chr8:74017934 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0210 a0001c0001t0001g0217 others(1): Show |
4 | HG03927.hp1 NA18979.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+7805C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017934 | |||||||
| chr8:74017997 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+7868C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74017997 | |||||||
| chr8:74018129 | G | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+8000G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018129 | |||||||
| chr8:74018130 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+8001T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018130 | |||||||
| chr8:74018228 | C | CA | 69 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(66): Show |
70 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.331+8108dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74018228 | ||||||
| chr8:74018252 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0114 a0001c0001t0001g0142 |
3 | NA18951.hp2 NA18986.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.331+8123A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018252 | |||||||
| chr8:74018284 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.331+8155T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018284 | |||||||
| chr8:74018344 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.331+8215A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018344 | |||||||
| chr8:74018456 | T | A | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+8327T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018456 | |||||||
| chr8:74018628 | C | G | 8 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(5): Show |
10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.332-8161C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018628 | |||||||
| chr8:74018659 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332-8130C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018659 | |||||||
| chr8:74018743 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-8046C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018743 | |||||||
| chr8:74018757 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-8032G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018757 | |||||||
| chr8:74018916 | T | G | 7 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.332-7873T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74018916 | |||||||
| chr8:74019089 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-7700G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019089 | |||||||
| chr8:74019248 | T | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.332-7541T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019248 | |||||||
| chr8:74019378 | C | T | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(1): Show |
4 | NA18967.hp1 NA19011.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-7411C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019378 | |||||||
| chr8:74019470 | C | T | 13 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(10): Show |
13 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-7319C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019470 | |||||||
| chr8:74019655 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-7134G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019655 | |||||||
| chr8:74019734 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.332-7055G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019734 | |||||||
| chr8:74019769 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.332-7020C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019769 | |||||||
| chr8:74019877 | A | G | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-6912A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019877 | |||||||
| chr8:74019902 | C | G | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.332-6887C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019902 | |||||||
| chr8:74019915 | G | A | 20 | a0001c0001t0001g0161 a0001c0001t0001g0199 a0001c0001t0001g0200 others(17): Show |
20 | HG01069.hp1 HG01081.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.332-6874G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019915 | |||||||
| chr8:74019921 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01258.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.332-6868C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74019921 | |||||||
| chr8:74020084 | G | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.332-6705G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020084 | |||||||
| chr8:74020100 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0265 a0001c0001t0002g0299 |
3 | HG02145.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.332-6689T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020100 | |||||||
| chr8:74020145 | T | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0079 others(2): Show |
5 | HG00438.hp1 NA18979.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-6644T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020145 | |||||||
| chr8:74020206 | A | G | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-6583A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020206 | |||||||
| chr8:74020243 | G | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-6546G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020243 | |||||||
| chr8:74020430 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.332-6359A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020430 | |||||||
| chr8:74020518 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.332-6271C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74020518 | |||||||
| chr8:74021017 | C | T | 98 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.332-5772C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021017 | |||||||
| chr8:74021189 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-5600T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021189 | |||||||
| chr8:74021213 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.332-5576C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021213 | |||||||
| chr8:74021344 | A | G | 67 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.332-5445A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021344 | |||||||
| chr8:74021355 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.332-5434T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021355 | |||||||
| chr8:74021523 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.332-5266A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021523 | |||||||
| chr8:74021622 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.332-5167G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021622 | |||||||
| chr8:74021684 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.332-5105A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021684 | |||||||
| chr8:74021733 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.332-5056A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021733 | |||||||
| chr8:74021806 | C | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-4983C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021806 | |||||||
| chr8:74021821 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.332-4968A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021821 | |||||||
| chr8:74021828 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0291 |
2 | HG01496.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.332-4961A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021828 | |||||||
| chr8:74021838 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-4951G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021838 | |||||||
| chr8:74021976 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-4813C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74021976 | |||||||
| chr8:74022021 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.332-4768G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022021 | |||||||
| chr8:74022072 | T | TA | 27 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(24): Show |
29 | HG01081.hp1 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.332-4707dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74022072 | ||||||
| chr8:74022102 | G | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.332-4687G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022102 | |||||||
| chr8:74022136 | A | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-4653A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022136 | |||||||
| chr8:74022145 | A | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-4644A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022145 | |||||||
| chr8:74022178 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.332-4611C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022178 | |||||||
| chr8:74022301 | C | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(65): Show |
69 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.332-4488C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022301 | |||||||
| chr8:74022303 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-4486G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022303 | |||||||
| chr8:74022422 | C | CA | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-4358dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74022422 | ||||||
| chr8:74022467 | C | CA | 126 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(123): Show |
129 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.332-4312dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74022467 | ||||||
| chr8:74022479 | G | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0168 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-4310G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022479 | |||||||
| chr8:74022491 | C | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0284 |
2 | HG01433.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.332-4298C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022491 | |||||||
| chr8:74022581 | C | CTT | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-4194_332-4193d others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74022581 | ||||||
| chr8:74022648 | A | C | 129 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(126): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.332-4141A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022648 | |||||||
| chr8:74022649 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-4140G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022649 | |||||||
| chr8:74022688 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.332-4101C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022688 | |||||||
| chr8:74022689 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.332-4100C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022689 | |||||||
| chr8:74022727 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-4062T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022727 | |||||||
| chr8:74022831 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.332-3958G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022831 | |||||||
| chr8:74022995 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-3794C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74022995 | |||||||
| chr8:74023074 | G | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-3715G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023074 | |||||||
| chr8:74023145 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.332-3644C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023145 | |||||||
| chr8:74023173 | G | T | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-3616G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023173 | |||||||
| chr8:74023281 | G | T | 3 | a0001c0001t0001g0242 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | NA18941.hp2 NA19083.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.332-3508G>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023281 | |||||||
| chr8:74023338 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-3451A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023338 | |||||||
| chr8:74023376 | G | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.332-3413G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023376 | |||||||
| chr8:74023438 | T | G | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-3351T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023438 | |||||||
| chr8:74023464 | C | T | 98 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.332-3325C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023464 | |||||||
| chr8:74023559 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.332-3230C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023559 | |||||||
| chr8:74023573 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-3216C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023573 | |||||||
| chr8:74023854 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG02257.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.332-2935T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74023854 | |||||||
| chr8:74024261 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.332-2528A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024261 | |||||||
| chr8:74024457 | G | A | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-2332G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024457 | |||||||
| chr8:74024513 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-2276A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024513 | |||||||
| chr8:74024575 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.332-2214C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024575 | |||||||
| chr8:74024593 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-2196C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024593 | |||||||
| chr8:74024594 | G | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.332-2195G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024594 | |||||||
| chr8:74024640 | T | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-2149T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024640 | |||||||
| chr8:74024665 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-2124C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024665 | |||||||
| chr8:74024678 | C | G | 1 | a0001c0001t0002g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.332-2111C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024678 | |||||||
| chr8:74024705 | A | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01167.hp2 HG01884.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-2084A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024705 | |||||||
| chr8:74024788 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.332-2001A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024788 | |||||||
| chr8:74024829 | A | G | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-1960A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024829 | |||||||
| chr8:74024932 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-1857A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024932 | |||||||
| chr8:74024943 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.332-1846C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74024943 | |||||||
| chr8:74025038 | G | C | 4 | a0001c0001t0001g0264 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG02735.hp1 NA19000.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1751G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025038 | |||||||
| chr8:74025170 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-1619C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025170 | |||||||
| chr8:74025203 | G | C | 13 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(10): Show |
13 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-1586G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025203 | |||||||
| chr8:74025372 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.332-1417C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025372 | |||||||
| chr8:74025388 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-1401T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025388 | |||||||
| chr8:74025641 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.332-1148C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025641 | |||||||
| chr8:74025654 | C | CA | 9 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0126 others(6): Show |
9 | HG00099.hp2 HG01106.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.332-1114dupA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74025654 | ||||||
| chr8:74025654 | C | CAAA | 13 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(10): Show |
15 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.332-1116_332-1114d others(5): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74025654 | ||||||
| chr8:74025654 | C | CAAAA | 12 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(9): Show |
12 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-1117_332-1114d others(6): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74025654 | ||||||
| chr8:74025654 | CA | C | 95 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(92): Show |
96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.332-1114delA | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74025654 | ||||||
| chr8:74025733 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332-1056C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025733 | |||||||
| chr8:74025735 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332-1054C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025735 | |||||||
| chr8:74025838 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332-951T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025838 | |||||||
| chr8:74025865 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332-924G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025865 | |||||||
| chr8:74025977 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-812C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74025977 | |||||||
| chr8:74026100 | A | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332-689A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026100 | |||||||
| chr8:74026145 | C | CTATT | 98 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.332-641_332-640ins others(4): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 74026145 | ||||||
| chr8:74026149 | A | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-640A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026149 | |||||||
| chr8:74026150 | T | TATA | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-639_332-638ins others(3): Show |
LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026150 | |||||||
| chr8:74026152 | A | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-637A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026152 | |||||||
| chr8:74026206 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.332-583A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026206 | |||||||
| chr8:74026291 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.332-498A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026291 | |||||||
| chr8:74026467 | T | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-322T>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026467 | |||||||
| chr8:74026468 | A | T | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-321A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026468 | |||||||
| chr8:74026469 | G | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-320G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026469 | |||||||
| chr8:74026471 | T | C | 12 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(9): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-318T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026471 | |||||||
| chr8:74026630 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.332-159A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026630 | |||||||
| chr8:74026661 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.332-128T>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 3/4 | chr8 | 74026661 | |||||||
| chr8:74026956 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.384+115T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74026956 | |||||||
| chr8:74027024 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384+183G>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74027024 | |||||||
| chr8:74027311 | C | CT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0143 others(7): Show |
10 | HG00735.hp1 HG01515.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+487dupT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 74027311 | ||||||
| chr8:74027311 | CT | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
19 | HG01069.hp2 HG01346.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.384+487delT | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 74027311 | ||||||
| chr8:74027439 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.384+598G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74027439 | |||||||
| chr8:74027829 | A | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0014 others(26): Show |
31 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.384+988A>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74027829 | |||||||
| chr8:74027865 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.384+1024G>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74027865 | |||||||
| chr8:74028276 | T | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.385-680T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028276 | |||||||
| chr8:74028388 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.385-568C>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028388 | |||||||
| chr8:74028455 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385-501T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028455 | |||||||
| chr8:74028472 | T | C | 10 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0023 others(7): Show |
12 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.385-484T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028472 | |||||||
| chr8:74028651 | A | T | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.385-305A>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028651 | |||||||
| chr8:74028658 | C | A | 1 | a0001c0001t0002g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385-298C>A | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028658 | |||||||
| chr8:74028771 | T | C | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.385-185T>C | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028771 | |||||||
| chr8:74028883 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.385-73A>G | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028883 | |||||||
| chr8:74028948 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.385-8C>T | LY96 | ENSG00000154589.7 | transcript | ENST00000284818.7 | protein_coding | 4/4 | chr8 | 74028948 |