Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23531 |
| ensemblid | ENSG00000108960.9 |
| hgncid | 7153 |
| symbol | MMD |
| name | monocyte to macrophage differentiation associated |
| refseq_nuc | NM_012329.3 |
| refseq_prot | NP_036461.2 |
| ensembl_nuc | ENST00000262065.8 |
| ensembl_prot | ENSP00000262065.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 55392622 |
| end | 55421835 |
| strand | - |
| ver | v1.2 |
| region | chr17:55392622-55421835 |
| region5000 | chr17:55387622-55426835 |
| regionname0 | MMD_chr17_55392622_55421835 |
| regionname5000 | MMD_chr17_55387622_55426835 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 714 | 393 | 81 | 69 | 178 | 16 | 47 | MMD_chr17_55387622_55426835 | MMD | ATGCG others(709): Show |
chr17 | 55387622 | 55426835 | ||
| a0001c0002 | 0/0 | 714 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ATGCG others(709): Show |
chr17 | 55387622 | 55426835 | ||
| a0001c0003 | 0/0 | 714 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ATGCG others(709): Show |
chr17 | 55387622 | 55426835 | ||
| a0001c0004 | 0/0 | 714 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | ATGCG others(709): Show |
chr17 | 55387622 | 55426835 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2569 | 142 | 39 | 16 | 73 | 1 | 12 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0002 | 0/1 | 2568 | 63 | 3 | 27 | 19 | 4 | 9 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0003 | 0/0 | 2568 | 62 | 4 | 13 | 25 | 8 | 12 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0004 | 0/0 | 2567 | 53 | 0 | 2 | 42 | 0 | 9 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2562): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0005 | 0/0 | 2568 | 12 | 0 | 7 | 0 | 3 | 2 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0006 | 0/0 | 2569 | 11 | 0 | 0 | 10 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0007 | 0/0 | 2568 | 11 | 11 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0009 | 0/0 | 2568 | 7 | 6 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0010 | 0/0 | 2567 | 7 | 6 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2562): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0011 | 0/0 | 2568 | 7 | 0 | 0 | 7 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0012 | 0/0 | 2567 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2562): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0013 | 0/0 | 2568 | 3 | 2 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0014 | 0/0 | 2569 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0015 | 0/0 | 2569 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0016 | 0/0 | 2569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0017 | 0/0 | 2569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0018 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0019 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0020 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0021 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0022 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0023 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2562): Show |
chr17 | 55387622 | 55426835 |
| a0001c0001t0024 | 0/0 | 2569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0002t0008 | 0/0 | 2569 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| a0001c0003t0009 | 0/0 | 2568 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2563): Show |
chr17 | 55387622 | 55426835 |
| a0001c0004t0001 | 0/0 | 2569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | ACTCC others(2564): Show |
chr17 | 55387622 | 55426835 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 45 | 0 | 6 | 36 | 1 | 2 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0004 | 0/0 | 10 | 0 | 1 | 6 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0012 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0029 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0002 | 0/0 | 19 | 0 | 1 | 8 | 5 | 5 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0003 | 0/0 | 18 | 0 | 0 | 17 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0009g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0010g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0010g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0011g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0011g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0013g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0013g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0015g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0017g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0018g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0020g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0021g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0022g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0023g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0001t0024g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0002t0008g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0002t0008g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0002t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0002t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0003t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0003t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0003t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0222 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0202 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0149 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0211 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0132 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0031 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0220 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0209 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01109 | hp1 | a0001 | c0002 | t0008 | g0010 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0208 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0013 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0195 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0164 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0210 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02055 | hp2 | a0001 | c0002 | t0008 | g0010 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0110 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0214 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02135 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02148 | hp1 | a0001 | c0001 | t0010 | g0191 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02257 | hp2 | a0001 | c0002 | t0008 | g0088 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02258 | hp1 | a0001 | c0001 | t0023 | g0206 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0176 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02622 | hp2 | a0001 | c0001 | t0021 | g0138 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02717 | hp1 | a0001 | c0002 | t0008 | g0089 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02723 | hp1 | a0001 | c0002 | t0008 | g0021 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0177 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0207 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0087 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0096 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02896 | hp1 | a0001 | c0003 | t0009 | g0074 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0080 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02897 | hp1 | a0001 | c0003 | t0009 | g0075 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0143 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0079 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03710 | hp2 | a0001 | c0001 | t0018 | g0158 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0070 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0129 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0067 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0124 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | STU | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18522 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0031 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18943 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18956 | hp2 | a0001 | c0001 | t0011 | g0198 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18981 | hp1 | a0001 | c0001 | t0017 | g0115 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18985 | hp1 | a0001 | c0001 | t0024 | g0077 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0101 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19030 | hp2 | a0001 | c0001 | t0020 | g0186 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19070 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19080 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19089 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0185 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0146 | AFR | ASW | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ASW | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0027 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20905 | hp1 | a0001 | c0001 | t0016 | g0100 | SAS | GIH | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG01123 | hp2 | a0001 | c0001 | t0015 | g0099 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0190 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02486 | hp1 | a0001 | c0003 | t0009 | g0055 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0084 | AFR | USA | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | USA | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA21309 | hp1 | a0001 | c0002 | t0008 | g0086 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0194 | REF | REF | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0167 | REF | REF | MMD_chr17_55387622_55426835 | MMD | chr17 | 55387622 | 55426835 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55394523 | A | G | 1 | a0001c0002 | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
synonymous_variant | LOW | c.528T>C | p.Asp176Asp | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 668/2569 | 528/717 | 176/238 | chr17 | 55394523 | |||
| chr17:55411322 | T | A | 1 | a0001c0004 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.204A>T | p.Gly68Gly | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/7 | 344/2569 | 204/717 | 68/238 | chr17 | 55411322 | |||
| chr17:55411403 | C | T | 1 | a0001c0003 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/7 | 263/2569 | 123/717 | 41/238 | chr17 | 55411403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55392643 | A | G | 1 | a0001c0001t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1691T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1691 | chr17 | 55392643 | ||||||
| chr17:55392739 | T | G | 1 | a0001c0001t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1595 | chr17 | 55392739 | ||||||
| chr17:55392933 | G | T | 1 | a0001c0001t0014 | 2 | HG02818.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1401C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1401 | chr17 | 55392933 | ||||||
| chr17:55392964 | G | C | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0019 others(1): Show |
16 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1370C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1370 | chr17 | 55392964 | ||||||
| chr17:55393037 | G | A | 1 | a0001c0001t0011 | 7 | HG02132.hp1 HG02135.hp2 NA18943.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1297C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1297 | chr17 | 55393037 | ||||||
| chr17:55393054 | A | G | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1280T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1280 | chr17 | 55393054 | ||||||
| chr17:55393101 | C | T | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(6): Show |
138 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1233G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1233 | chr17 | 55393101 | ||||||
| chr17:55393202 | G | T | 1 | a0001c0001t0018 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1132 | chr17 | 55393202 | ||||||
| chr17:55393251 | GA | G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(8): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1082delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1082 | chr17 | 55393251 | ||||||
| chr17:55393251 | GAA | G | 4 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0012 others(1): Show |
64 | HG00735.hp2 HG01123.hp1 HG01891.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1081_*1082delTT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1081 | chr17 | 55393251 | ||||||
| chr17:55393266 | A | C | 1 | a0001c0001t0006 | 11 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1068T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1068 | chr17 | 55393266 | ||||||
| chr17:55393658 | G | A | 1 | a0001c0002t0008 | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*676C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 676 | chr17 | 55393658 | ||||||
| chr17:55393744 | T | G | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(3): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 590 | chr17 | 55393744 | ||||||
| chr17:55393815 | A | T | 1 | a0001c0001t0017 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 519 | chr17 | 55393815 | ||||||
| chr17:55393830 | T | A | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(2): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 504 | chr17 | 55393830 | ||||||
| chr17:55393897 | T | C | 1 | a0001c0001t0013 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 437 | chr17 | 55393897 | ||||||
| chr17:55394146 | C | T | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG01123.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 188 | chr17 | 55394146 | ||||||
| chr17:55394214 | C | G | 1 | a0001c0001t0015 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 120 | chr17 | 55394214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55394595 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517-61T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394595 | |||||||
| chr17:55394858 | G | A | 1 | a0001c0001t0001g0008 | 6 | NA18747.hp1 NA18960.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-324C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394858 | |||||||
| chr17:55394898 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0040 |
4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-364G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394898 | |||||||
| chr17:55395539 | G | T | 1 | a0001c0001t0005g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.517-1005C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395539 | |||||||
| chr17:55395575 | T | C | 1 | a0001c0001t0006g0110 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-1041A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395575 | |||||||
| chr17:55395637 | T | A | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.517-1103A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395637 | |||||||
| chr17:55395648 | C | T | 1 | a0001c0001t0005g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.517-1114G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395648 | |||||||
| chr17:55395728 | A | G | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.517-1194T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395728 | |||||||
| chr17:55395797 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517-1263A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395797 | |||||||
| chr17:55396076 | C | T | 1 | a0001c0001t0003g0042 | 2 | HG01074.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.517-1542G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396076 | |||||||
| chr17:55396207 | A | G | 1 | a0001c0001t0018g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.517-1673T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396207 | |||||||
| chr17:55396347 | C | T | 1 | a0001c0001t0003g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.517-1813G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396347 | |||||||
| chr17:55396535 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.517-2001A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396535 | |||||||
| chr17:55396556 | T | C | 1 | a0001c0001t0005g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-2022A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396556 | |||||||
| chr17:55396601 | T | G | 5 | a0001c0001t0001g0117 a0001c0001t0002g0047 a0001c0001t0002g0192 others(2): Show |
6 | HG01261.hp1 HG01496.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-2067A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396601 | |||||||
| chr17:55396604 | G | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(60): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.517-2070C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396604 | |||||||
| chr17:55396607 | G | T | 39 | a0001c0001t0001g0175 a0001c0001t0003g0002 a0001c0001t0003g0041 others(36): Show |
63 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-2073C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396607 | |||||||
| chr17:55396622 | CT | C | 6 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0157 others(3): Show |
6 | HG01934.hp1 HG01993.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-2089delA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396622 | |||||||
| chr17:55396639 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517-2105A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396639 | |||||||
| chr17:55396675 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.517-2141C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396675 | |||||||
| chr17:55396677 | A | G | 3 | a0001c0003t0009g0055 a0001c0003t0009g0074 a0001c0003t0009g0075 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.517-2143T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396677 | |||||||
| chr17:55396761 | C | T | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.517-2227G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396761 | |||||||
| chr17:55396775 | C | T | 2 | a0001c0001t0003g0162 a0001c0001t0018g0158 |
2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.517-2241G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396775 | |||||||
| chr17:55396830 | T | C | 1 | a0001c0001t0007g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.517-2296A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396830 | |||||||
| chr17:55396906 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.517-2372G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396906 | |||||||
| chr17:55397159 | G | GTTTA | 2 | a0001c0001t0010g0023 a0001c0001t0010g0190 |
4 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2629_517-2626d others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397159 | |||||||
| chr17:55397165 | T | G | 2 | a0001c0001t0013g0031 a0001c0001t0013g0080 |
3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517-2631A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397165 | |||||||
| chr17:55397387 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.517-2853G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397387 | |||||||
| chr17:55397391 | C | T | 1 | a0001c0001t0005g0027 | 3 | HG01175.hp1 HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.517-2857G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397391 | |||||||
| chr17:55397478 | C | T | 176 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(173): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.517-2944G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397478 | |||||||
| chr17:55397557 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517-3023A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397557 | |||||||
| chr17:55397617 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0103 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.517-3083G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397617 | |||||||
| chr17:55397665 | C | T | 1 | a0001c0001t0012g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-3131G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397665 | |||||||
| chr17:55397680 | A | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-3146T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397680 | |||||||
| chr17:55397687 | T | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(95): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.517-3153A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397687 | |||||||
| chr17:55397703 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(95): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.517-3169T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397703 | |||||||
| chr17:55397788 | C | T | 1 | a0001c0001t0002g0049 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517-3254G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397788 | |||||||
| chr17:55397849 | CA | C | 5 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0179 others(2): Show |
8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-3316delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397849 | |||||||
| chr17:55397863 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0205 a0001c0001t0002g0218 others(1): Show |
7 | HG00558.hp2 NA18953.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-3329G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397863 | |||||||
| chr17:55397934 | T | TTC | 4 | a0001c0001t0004g0014 a0001c0001t0004g0063 a0001c0001t0004g0066 others(1): Show |
7 | HG00735.hp2 HG02015.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-3402_517-3401d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397934 | |||||||
| chr17:55397954 | A | G | 3 | a0001c0001t0009g0013 a0001c0001t0009g0056 a0001c0001t0009g0096 |
6 | HG01243.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-3420T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397954 | |||||||
| chr17:55397974 | G | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0204 |
2 | HG00639.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.517-3440C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397974 | |||||||
| chr17:55398111 | C | CA | 73 | a0001c0001t0001g0054 a0001c0001t0001g0121 a0001c0001t0002g0004 others(70): Show |
142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.516+3357dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | |||||||
| chr17:55398111 | C | CAA | 23 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(20): Show |
26 | HG01433.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.516+3356_516+3357d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | |||||||
| chr17:55398111 | CAAAA | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(62): Show |
115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.516+3354_516+3357d others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | |||||||
| chr17:55398126 | A | AG | 2 | a0001c0001t0002g0015 a0001c0001t0002g0078 |
5 | HG00140.hp1 HG01070.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+3342_516+3343i others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398126 | |||||||
| chr17:55398126 | A | G | 1 | a0001c0001t0006g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.516+3343T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398126 | |||||||
| chr17:55398254 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.516+3215C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398254 | |||||||
| chr17:55398331 | A | C | 1 | a0001c0001t0006g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+3138T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398331 | |||||||
| chr17:55398377 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516+3092A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398377 | |||||||
| chr17:55398473 | C | G | 3 | a0001c0001t0004g0006 a0001c0001t0004g0061 a0001c0001t0004g0065 |
8 | NA18953.hp2 NA18961.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+2996G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398473 | |||||||
| chr17:55398566 | G | T | 3 | a0001c0003t0009g0055 a0001c0003t0009g0074 a0001c0003t0009g0075 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.516+2903C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398566 | |||||||
| chr17:55398568 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.516+2901A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398568 | |||||||
| chr17:55398592 | T | C | 1 | a0001c0001t0022g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.516+2877A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398592 | |||||||
| chr17:55398649 | A | C | 1 | a0001c0001t0005g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.516+2820T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398649 | |||||||
| chr17:55398876 | C | A | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.516+2593G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398876 | |||||||
| chr17:55398969 | G | A | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+2500C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398969 | |||||||
| chr17:55399038 | A | G | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+2431T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399038 | |||||||
| chr17:55399246 | CA | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(83): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.516+2222delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399246 | |||||||
| chr17:55399251 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+2218T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399251 | |||||||
| chr17:55399316 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.516+2153G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399316 | |||||||
| chr17:55399562 | G | A | 5 | a0001c0002t0008g0010 a0001c0002t0008g0021 a0001c0002t0008g0086 others(2): Show |
11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+1907C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399562 | |||||||
| chr17:55399564 | C | A | 42 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0003g0002 others(39): Show |
66 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.516+1905G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399564 | |||||||
| chr17:55399613 | A | G | 1 | a0001c0002t0008g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.516+1856T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399613 | |||||||
| chr17:55399677 | A | G | 176 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(173): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.516+1792T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399677 | |||||||
| chr17:55399794 | G | A | 1 | a0001c0001t0002g0033 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.516+1675C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399794 | |||||||
| chr17:55399961 | C | T | 14 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(11): Show |
19 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+1508G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399961 | |||||||
| chr17:55400060 | T | C | 4 | a0001c0001t0010g0023 a0001c0001t0010g0147 a0001c0001t0010g0148 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1409A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400060 | |||||||
| chr17:55400129 | G | A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(55): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.516+1340C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400129 | |||||||
| chr17:55400155 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0178 others(5): Show |
12 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+1314A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400155 | |||||||
| chr17:55400225 | T | C | 55 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0178 others(52): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.516+1244A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400225 | |||||||
| chr17:55400399 | A | C | 5 | a0001c0001t0007g0141 a0001c0001t0007g0185 a0001c0001t0012g0084 others(2): Show |
5 | HG02451.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+1070T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400399 | |||||||
| chr17:55400401 | T | C | 47 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0012 others(44): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.516+1068A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400401 | |||||||
| chr17:55400481 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.516+988C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400481 | |||||||
| chr17:55400556 | G | GA | 166 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(163): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.516+912dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400556 | |||||||
| chr17:55400662 | T | C | 1 | a0001c0001t0004g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.516+807A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400662 | |||||||
| chr17:55400757 | G | A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(55): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.516+712C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400757 | |||||||
| chr17:55401051 | G | A | 14 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(11): Show |
19 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+418C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401051 | |||||||
| chr17:55401174 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG03139.hp1 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+295A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401174 | |||||||
| chr17:55401314 | A | G | 176 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(173): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.516+155T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401314 | |||||||
| chr17:55401375 | A | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+94T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401375 | |||||||
| chr17:55401618 | T | C | 1 | a0001c0001t0002g0048 | 2 | HG00733.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.447-80A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401618 | |||||||
| chr17:55401705 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(66): Show |
114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.447-167G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401705 | |||||||
| chr17:55401737 | C | T | 4 | a0001c0001t0010g0023 a0001c0001t0010g0147 a0001c0001t0010g0148 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.447-199G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401737 | |||||||
| chr17:55401739 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.447-201G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401739 | |||||||
| chr17:55401879 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.447-341G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401879 | |||||||
| chr17:55401978 | AGAATGGC others(8): Show |
A | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(118): Show |
207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.447-455_447-441del others(15): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401978 | |||||||
| chr17:55402087 | C | CA | 27 | a0001c0001t0001g0139 a0001c0001t0002g0033 a0001c0001t0002g0050 others(24): Show |
37 | HG00323.hp1 HG00558.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.447-550dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402087 | |||||||
| chr17:55402087 | CA | C | 76 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(73): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.447-550delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402087 | |||||||
| chr17:55402104 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-566T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402104 | |||||||
| chr17:55402105 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-567C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402105 | |||||||
| chr17:55402134 | G | C | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.447-596C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402134 | |||||||
| chr17:55402136 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.447-598G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402136 | |||||||
| chr17:55402186 | C | T | 46 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0012 others(43): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.447-648G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402186 | |||||||
| chr17:55402260 | T | C | 10 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(7): Show |
13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.447-722A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402260 | |||||||
| chr17:55402678 | C | T | 4 | a0001c0001t0010g0023 a0001c0001t0010g0147 a0001c0001t0010g0148 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.446+1089G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402678 | |||||||
| chr17:55402812 | T | C | 1 | a0001c0001t0003g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.446+955A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402812 | |||||||
| chr17:55402965 | C | T | 10 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(7): Show |
13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.446+802G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402965 | |||||||
| chr17:55403056 | A | T | 1 | a0001c0001t0005g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.446+711T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403056 | |||||||
| chr17:55403159 | A | T | 1 | a0001c0001t0004g0071 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.446+608T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403159 | |||||||
| chr17:55403231 | A | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.446+536T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403231 | |||||||
| chr17:55403453 | G | A | 1 | a0001c0001t0010g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.446+314C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403453 | |||||||
| chr17:55403655 | T | C | 5 | a0001c0001t0007g0141 a0001c0001t0007g0185 a0001c0001t0012g0084 others(2): Show |
5 | HG02451.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+112A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403655 | |||||||
| chr17:55403698 | G | A | 3 | a0001c0001t0009g0013 a0001c0001t0009g0056 a0001c0001t0009g0096 |
6 | HG01243.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+69C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403698 | |||||||
| chr17:55403902 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.345-34C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55403902 | |||||||
| chr17:55404291 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0001g0134 others(1): Show |
5 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-423C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404291 | |||||||
| chr17:55404319 | C | A | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.345-451G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404319 | |||||||
| chr17:55404330 | G | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(41): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-462C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404330 | |||||||
| chr17:55404415 | G | A | 5 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0179 others(2): Show |
8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-547C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404415 | |||||||
| chr17:55404443 | C | T | 28 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0014 others(25): Show |
62 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.345-575G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404443 | |||||||
| chr17:55404565 | C | T | 1 | a0001c0001t0003g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-697G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404565 | |||||||
| chr17:55404588 | G | C | 3 | a0001c0001t0007g0091 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.345-720C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404588 | |||||||
| chr17:55404836 | C | A | 1 | a0001c0001t0003g0168 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.345-968G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404836 | |||||||
| chr17:55404889 | C | T | 1 | a0001c0001t0006g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.345-1021G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404889 | |||||||
| chr17:55405070 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.345-1202A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405070 | |||||||
| chr17:55405197 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | NA18997.hp2 NA19072.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1329T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405197 | |||||||
| chr17:55405379 | GA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(72): Show |
169 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.345-1512delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405379 | |||||||
| chr17:55405379 | GAA | G | 46 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0012 others(43): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.345-1513_345-1512d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405379 | |||||||
| chr17:55405653 | G | T | 4 | a0001c0001t0010g0023 a0001c0001t0010g0147 a0001c0001t0010g0148 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1785C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405653 | |||||||
| chr17:55405666 | C | T | 4 | a0001c0001t0010g0023 a0001c0001t0010g0147 a0001c0001t0010g0148 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1798G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405666 | |||||||
| chr17:55405678 | C | G | 1 | a0001c0001t0003g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.345-1810G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405678 | |||||||
| chr17:55405687 | GTTC | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(118): Show |
252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.345-1822_345-1820d others(5): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405687 | |||||||
| chr17:55405751 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(41): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-1883A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405751 | |||||||
| chr17:55405936 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.344+1810T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405936 | |||||||
| chr17:55406022 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.344+1724T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406022 | |||||||
| chr17:55406103 | TTCAAAAA others(18): Show |
T | 15 | a0001c0001t0003g0098 a0001c0001t0007g0025 a0001c0001t0007g0030 others(12): Show |
20 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.344+1618_344+1642d others(27): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406103 | |||||||
| chr17:55406149 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.344+1597G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406149 | |||||||
| chr17:55406263 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(7): Show |
23 | HG00544.hp2 HG00597.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.344+1483G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406263 | |||||||
| chr17:55406313 | G | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.344+1433C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406313 | |||||||
| chr17:55406408 | C | G | 34 | a0001c0001t0001g0022 a0001c0001t0001g0136 a0001c0001t0001g0137 others(31): Show |
70 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.344+1338G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406408 | |||||||
| chr17:55406535 | T | C | 1 | a0001c0001t0004g0069 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.344+1211A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406535 | |||||||
| chr17:55406551 | T | C | 1 | a0001c0001t0006g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.344+1195A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406551 | |||||||
| chr17:55406610 | G | A | 10 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(7): Show |
13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+1136C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406610 | |||||||
| chr17:55406620 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(133): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.344+1126T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406620 | |||||||
| chr17:55406629 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(41): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1117G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406629 | |||||||
| chr17:55406695 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(41): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1051C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406695 | |||||||
| chr17:55406701 | A | G | 1 | a0001c0001t0007g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.344+1045T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406701 | |||||||
| chr17:55406710 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(41): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1036G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406710 | |||||||
| chr17:55406743 | C | A | 1 | a0001c0001t0006g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.344+1003G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406743 | |||||||
| chr17:55406842 | C | T | 5 | a0001c0002t0008g0010 a0001c0002t0008g0021 a0001c0002t0008g0086 others(2): Show |
11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+904G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406842 | |||||||
| chr17:55406858 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344+888G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406858 | |||||||
| chr17:55407142 | A | G | 1 | a0001c0001t0003g0171 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.344+604T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407142 | |||||||
| chr17:55407149 | T | C | 1 | a0001c0001t0022g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344+597A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407149 | |||||||
| chr17:55407158 | G | A | 10 | a0001c0001t0007g0025 a0001c0001t0007g0030 a0001c0001t0007g0141 others(7): Show |
13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+588C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407158 | |||||||
| chr17:55407229 | T | C | 13 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+517A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407229 | |||||||
| chr17:55407237 | G | A | 1 | a0001c0001t0006g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.344+509C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407237 | |||||||
| chr17:55407298 | C | CTAAA | 3 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0083 |
3 | HG02258.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.344+447_344+448ins others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407298 | |||||||
| chr17:55407299 | A | AAAAT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0094 others(9): Show |
22 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+443_344+446dup others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | A | AAAATAAA others(1): Show |
3 | a0001c0001t0014g0087 a0001c0001t0018g0158 a0001c0002t0008g0086 |
3 | HG02818.hp1 HG03710.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.344+439_344+446dup others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | A | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG02258.hp2 HG02451.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+447T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | AAAAT | A | 51 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0038 others(48): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.344+443_344+446del others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | AAAATAAA others(1): Show |
A | 11 | a0001c0001t0003g0098 a0001c0001t0007g0091 a0001c0001t0007g0142 others(8): Show |
11 | HG02486.hp1 HG02886.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+439_344+446del others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.344+435_344+446del others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407299 | AAAATAAA others(9): Show |
A | 33 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0014 others(30): Show |
69 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.344+431_344+446del others(16): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | |||||||
| chr17:55407327 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
8 | HG01891.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+419A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407327 | |||||||
| chr17:55407355 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.344+391G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407355 | |||||||
| chr17:55407391 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(178): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.344+355A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407391 | |||||||
| chr17:55407489 | C | T | 1 | a0001c0001t0022g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344+257G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407489 | |||||||
| chr17:55407490 | A | T | 4 | a0001c0001t0007g0091 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+256T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407490 | |||||||
| chr17:55407613 | A | G | 1 | a0001c0001t0007g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.344+133T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407613 | |||||||
| chr17:55407825 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(110): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
splice_region_variant&intron_variant | LOW | c.270-5G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55407825 | |||||||
| chr17:55407944 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-124A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55407944 | |||||||
| chr17:55408050 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-230T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408050 | |||||||
| chr17:55408056 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.270-236A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408056 | |||||||
| chr17:55408065 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(129): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.270-245C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408065 | |||||||
| chr17:55408197 | C | T | 1 | a0001c0001t0003g0043 | 2 | HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.270-377G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408197 | |||||||
| chr17:55408198 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0003g0174 |
2 | NA18981.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.270-378C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408198 | |||||||
| chr17:55408275 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-455G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408275 | |||||||
| chr17:55408382 | CA | C | 4 | a0001c0001t0007g0185 a0001c0001t0012g0084 a0001c0001t0012g0176 others(1): Show |
4 | HG02451.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-563delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408382 | |||||||
| chr17:55408388 | C | CA | 4 | a0001c0001t0007g0091 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-569dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408388 | |||||||
| chr17:55408458 | G | GA | 6 | a0001c0001t0001g0187 a0001c0001t0007g0025 a0001c0001t0007g0030 others(3): Show |
9 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.270-639dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408458 | |||||||
| chr17:55408654 | C | T | 3 | a0001c0003t0009g0055 a0001c0003t0009g0074 a0001c0003t0009g0075 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.270-834G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408654 | |||||||
| chr17:55408655 | G | A | 2 | a0001c0001t0006g0110 a0001c0001t0006g0111 |
2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.270-835C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408655 | |||||||
| chr17:55408874 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(43): Show |
106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.270-1054C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408874 | |||||||
| chr17:55408955 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.270-1135G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408955 | |||||||
| chr17:55409119 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.270-1299T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409119 | |||||||
| chr17:55409225 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270-1405G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409225 | |||||||
| chr17:55409400 | C | T | 2 | a0001c0001t0006g0110 a0001c0001t0006g0111 |
2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.270-1580G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409400 | |||||||
| chr17:55409443 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-1623T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409443 | |||||||
| chr17:55409453 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.270-1633G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409453 | |||||||
| chr17:55409563 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(139): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.269+1694C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409563 | |||||||
| chr17:55409715 | G | T | 1 | a0001c0001t0006g0109 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.269+1542C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409715 | |||||||
| chr17:55409722 | G | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(43): Show |
106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.269+1535C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409722 | |||||||
| chr17:55409786 | G | C | 1 | a0001c0001t0007g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.269+1471C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409786 | |||||||
| chr17:55409954 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.269+1303G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409954 | |||||||
| chr17:55409957 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(147): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.269+1300T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409957 | |||||||
| chr17:55410075 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.269+1182T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410075 | |||||||
| chr17:55410303 | A | C | 81 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(78): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.269+954T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410303 | |||||||
| chr17:55410348 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(53): Show |
116 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.269+909C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410348 | |||||||
| chr17:55410471 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.269+786T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410471 | |||||||
| chr17:55410567 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.269+690A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410567 | |||||||
| chr17:55410675 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(53): Show |
116 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.269+582G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410675 | |||||||
| chr17:55410707 | C | T | 6 | a0001c0001t0014g0087 a0001c0002t0008g0010 a0001c0002t0008g0021 others(3): Show |
12 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.269+550G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410707 | |||||||
| chr17:55410766 | A | G | 1 | a0001c0001t0022g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.269+491T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410766 | |||||||
| chr17:55410985 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.269+272C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410985 | |||||||
| chr17:55411044 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.269+213C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55411044 | |||||||
| chr17:55411640 | G | C | 26 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0014 others(23): Show |
58 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-223C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411640 | |||||||
| chr17:55411681 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(7): Show |
23 | HG00544.hp2 HG00597.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.109-264A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411681 | |||||||
| chr17:55411694 | G | GT | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-278_109-277ins others(1): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411694 | |||||||
| chr17:55411695 | G | T | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
61 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.109-278C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411695 | |||||||
| chr17:55411695 | GT | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(65): Show |
135 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.109-279delA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411695 | |||||||
| chr17:55411724 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0007g0025 a0001c0001t0007g0030 others(2): Show |
8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-307T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411724 | |||||||
| chr17:55411729 | G | A | 4 | a0001c0001t0007g0091 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-312C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411729 | |||||||
| chr17:55411826 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109-409G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411826 | |||||||
| chr17:55412212 | T | A | 1 | a0001c0001t0003g0170 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.109-795A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412212 | |||||||
| chr17:55412238 | G | A | 81 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(78): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.109-821C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412238 | |||||||
| chr17:55412863 | A | AT | 5 | a0001c0001t0001g0024 a0001c0001t0001g0178 a0001c0001t0001g0180 others(2): Show |
7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+1287dupA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412863 | |||||||
| chr17:55412932 | T | A | 21 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0014 others(18): Show |
50 | HG00735.hp2 HG01123.hp1 HG02015.hp1 others(47): Show |
intron_variant | MODIFIER | c.108+1219A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412932 | |||||||
| chr17:55412999 | C | T | 1 | a0001c0001t0012g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+1152G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412999 | |||||||
| chr17:55413000 | G | A | 1 | a0001c0001t0003g0171 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108+1151C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413000 | |||||||
| chr17:55413006 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1145T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413006 | |||||||
| chr17:55413026 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1125G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413026 | |||||||
| chr17:55413033 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1118T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413033 | |||||||
| chr17:55413040 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1111T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413040 | |||||||
| chr17:55413053 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1098G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413053 | |||||||
| chr17:55413058 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1093G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413058 | |||||||
| chr17:55413060 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1091G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413060 | |||||||
| chr17:55413061 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1090G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413061 | |||||||
| chr17:55413064 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1087A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413064 | |||||||
| chr17:55413065 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1086A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413065 | |||||||
| chr17:55413066 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1085T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413066 | |||||||
| chr17:55413069 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1082A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413069 | |||||||
| chr17:55413070 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1081T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413070 | |||||||
| chr17:55413071 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1080T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413071 | |||||||
| chr17:55413161 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+990T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413161 | |||||||
| chr17:55413167 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+984C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413167 | |||||||
| chr17:55413195 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0178 a0001c0001t0001g0180 others(2): Show |
7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+956A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413195 | |||||||
| chr17:55413205 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+946T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413205 | |||||||
| chr17:55413209 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+942A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413209 | |||||||
| chr17:55413211 | A | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+940T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413211 | |||||||
| chr17:55413219 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+932T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413219 | |||||||
| chr17:55413246 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+905T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413246 | |||||||
| chr17:55413248 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+903A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413248 | |||||||
| chr17:55413259 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+892G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413259 | |||||||
| chr17:55413273 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+878G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413273 | |||||||
| chr17:55413280 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+871A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413280 | |||||||
| chr17:55413281 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+870G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413281 | |||||||
| chr17:55413285 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+866A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413285 | |||||||
| chr17:55413286 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+865A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413286 | |||||||
| chr17:55413288 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+863A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413288 | |||||||
| chr17:55413289 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+862G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413289 | |||||||
| chr17:55413290 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+861T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413290 | |||||||
| chr17:55413292 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+859T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413292 | |||||||
| chr17:55413293 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+858G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413293 | |||||||
| chr17:55413294 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+857A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413294 | |||||||
| chr17:55413295 | G | T | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+856C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413295 | |||||||
| chr17:55413299 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+852G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413299 | |||||||
| chr17:55413300 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+851G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413300 | |||||||
| chr17:55413301 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+850G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413301 | |||||||
| chr17:55413310 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+841A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413310 | |||||||
| chr17:55413312 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+839A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413312 | |||||||
| chr17:55413318 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+833A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413318 | |||||||
| chr17:55413319 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+832G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413319 | |||||||
| chr17:55413322 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(172): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.108+829A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413322 | |||||||
| chr17:55413323 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.108+828C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413323 | |||||||
| chr17:55413464 | T | C | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
61 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.108+687A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413464 | |||||||
| chr17:55413674 | TCTC | T | 4 | a0001c0001t0007g0091 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+474_108+476del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413674 | |||||||
| chr17:55413704 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+447T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413704 | |||||||
| chr17:55413880 | A | G | 3 | a0001c0001t0002g0029 a0001c0001t0002g0195 a0001c0001t0002g0196 |
5 | HG01516.hp1 HG01934.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+271T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413880 | |||||||
| chr17:55414060 | C | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+91G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414060 | |||||||
| chr17:55414094 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(43): Show |
106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.108+57G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414094 | |||||||
| chr17:55414097 | C | T | 26 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0014 others(23): Show |
58 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+54G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414097 | |||||||
| chr17:55414142 | T | A | 1 | a0001c0001t0003g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.108+9A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414142 | |||||||
| chr17:55414448 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.27-216A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414448 | |||||||
| chr17:55414554 | A | G | 2 | a0001c0001t0013g0031 a0001c0001t0013g0080 |
3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-322T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414554 | |||||||
| chr17:55414555 | T | TACACAC | 3 | a0001c0003t0009g0055 a0001c0003t0009g0074 a0001c0003t0009g0075 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.27-324_27-323insGT others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414555 | |||||||
| chr17:55414555 | TTC | T | 2 | a0001c0001t0013g0031 a0001c0001t0013g0080 |
3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-325_27-324delGA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414555 | |||||||
| chr17:55414556 | T | A | 3 | a0001c0003t0009g0055 a0001c0003t0009g0074 a0001c0003t0009g0075 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.27-324A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0038 others(31): Show |
55 | HG00735.hp2 HG01123.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.27-326_27-325dupTG | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACA | 16 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
23 | HG00597.hp2 HG02004.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.27-328_27-325dupTG others(2): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACACA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(9): Show |
21 | HG00544.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-330_27-325dupTG others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACACAC others(1): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0097 others(3): Show |
7 | HG01167.hp1 HG02965.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-332_27-325dupTG others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACACAC others(3): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0182 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.27-334_27-325dupTG others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACACAC others(5): Show |
3 | a0001c0001t0001g0020 a0001c0001t0010g0023 a0001c0001t0010g0190 |
4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-336_27-325dupTG others(10): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | T | TCACACAC others(7): Show |
1 | a0001c0001t0010g0023 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27-338_27-325dupTG others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCA | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(52): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.27-326_27-325delTG | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCACA | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0082 others(77): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.27-328_27-325delTG others(2): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCACACA | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0219 others(1): Show |
4 | HG01256.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-330_27-325delTG others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27-334_27-325delTG others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.27-338_27-325delTG others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414556 | TCACACAC others(9): Show |
T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0136 a0001c0001t0001g0139 others(1): Show |
6 | HG01891.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-340_27-325delTG others(14): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | |||||||
| chr17:55414602 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.27-370A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414602 | |||||||
| chr17:55414610 | G | GA | 9 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
11 | HG00408.hp1 HG00597.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-379dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414610 | |||||||
| chr17:55414610 | GA | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
17 | HG02258.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-379delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414610 | |||||||
| chr17:55414620 | A | C | 1 | a0001c0001t0007g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.27-388T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414620 | |||||||
| chr17:55414643 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0003g0045 a0001c0001t0003g0152 others(1): Show |
5 | HG02132.hp2 NA18981.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-411A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414643 | |||||||
| chr17:55414721 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0178 a0001c0001t0001g0180 others(2): Show |
7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-489A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414721 | |||||||
| chr17:55415073 | C | T | 1 | a0001c0001t0009g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-841G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415073 | |||||||
| chr17:55415274 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-1042G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415274 | |||||||
| chr17:55415276 | TA | T | 28 | a0001c0001t0001g0090 a0001c0001t0001g0183 a0001c0001t0002g0193 others(25): Show |
60 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-1045delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415276 | |||||||
| chr17:55415377 | A | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-1145T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415377 | |||||||
| chr17:55415754 | TG | T | 6 | a0001c0001t0014g0087 a0001c0002t0008g0010 a0001c0002t0008g0021 others(3): Show |
12 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-1523delC | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415754 | |||||||
| chr17:55415837 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27-1605T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415837 | |||||||
| chr17:55416089 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.27-1857G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416089 | |||||||
| chr17:55416151 | T | C | 1 | a0001c0001t0007g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.27-1919A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416151 | |||||||
| chr17:55416352 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.27-2120G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416352 | |||||||
| chr17:55416371 | G | A | 1 | a0001c0001t0011g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.27-2139C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416371 | |||||||
| chr17:55416384 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.27-2152A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416384 | |||||||
| chr17:55416463 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2231A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416463 | |||||||
| chr17:55416579 | T | C | 6 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(3): Show |
12 | HG01070.hp2 HG01192.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.27-2347A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416579 | |||||||
| chr17:55416609 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.27-2377T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416609 | |||||||
| chr17:55416647 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
7 | HG01891.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-2415A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416647 | |||||||
| chr17:55416650 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2418T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416650 | |||||||
| chr17:55416653 | C | T | 1 | a0001c0003t0009g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27-2421G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416653 | |||||||
| chr17:55416710 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG02280.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.27-2478G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416710 | |||||||
| chr17:55416790 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.27-2558T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416790 | |||||||
| chr17:55416923 | T | G | 1 | a0001c0001t0022g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27-2691A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416923 | |||||||
| chr17:55416944 | C | T | 4 | a0001c0001t0007g0185 a0001c0001t0012g0084 a0001c0001t0012g0176 others(1): Show |
4 | HG02451.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2712G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416944 | |||||||
| chr17:55417045 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG03139.hp1 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-2813T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417045 | |||||||
| chr17:55417201 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.27-2969G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417201 | |||||||
| chr17:55417353 | C | T | 74 | a0001c0001t0001g0018 a0001c0001t0002g0004 a0001c0001t0002g0009 others(71): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.27-3121G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417353 | |||||||
| chr17:55417401 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.27-3169G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417401 | |||||||
| chr17:55417440 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-3208G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417440 | |||||||
| chr17:55417446 | T | A | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.27-3214A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417446 | |||||||
| chr17:55417633 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(174): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.27-3401T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417633 | |||||||
| chr17:55417706 | G | A | 1 | a0001c0001t0002g0029 | 3 | HG02055.hp1 HG03490.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.27-3474C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417706 | |||||||
| chr17:55417725 | G | A | 3 | a0001c0001t0007g0141 a0001c0001t0007g0142 a0001c0001t0019g0143 |
3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.27-3493C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417725 | |||||||
| chr17:55417959 | A | C | 1 | a0001c0001t0003g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.26+3711T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417959 | |||||||
| chr17:55417962 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.26+3708C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417962 | |||||||
| chr17:55418562 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.26+3108A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418562 | |||||||
| chr17:55418612 | C | T | 2 | a0001c0001t0013g0031 a0001c0001t0013g0080 |
3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.26+3058G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418612 | |||||||
| chr17:55418949 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26+2721A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418949 | |||||||
| chr17:55419326 | T | A | 1 | a0001c0001t0003g0046 | 2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.26+2344A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419326 | |||||||
| chr17:55419358 | A | G | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26+2312T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419358 | |||||||
| chr17:55419393 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+2277T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419393 | |||||||
| chr17:55419604 | GTAC | G | 76 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(73): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.26+2063_26+2065del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419604 | |||||||
| chr17:55419843 | C | T | 29 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0002g0073 others(26): Show |
63 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.26+1827G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419843 | |||||||
| chr17:55419885 | C | T | 74 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0002g0004 others(71): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.26+1785G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419885 | |||||||
| chr17:55419980 | TAAA | T | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.26+1687_26+1689del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419980 | |||||||
| chr17:55420243 | A | C | 2 | a0001c0001t0003g0041 a0001c0001t0003g0145 |
3 | NA18957.hp1 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.26+1427T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420243 | |||||||
| chr17:55420404 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(168): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.26+1266T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420404 | |||||||
| chr17:55420548 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.26+1122T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420548 | |||||||
| chr17:55420555 | T | TG | 19 | a0001c0001t0001g0024 a0001c0001t0001g0178 a0001c0001t0001g0180 others(16): Show |
25 | HG01081.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.26+1114dupC | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420555 | |||||||
| chr17:55420846 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+824A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420846 | |||||||
| chr17:55421307 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+363C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421307 | |||||||
| chr17:55421437 | G | A | 1 | a0001c0001t0010g0191 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.26+233C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421437 | |||||||
| chr17:55421485 | C | T | 47 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(44): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.26+185G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421485 | |||||||
| chr17:55421501 | C | G | 1 | a0001c0001t0013g0031 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26+169G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421501 | |||||||
| chr17:55421541 | TCCCTGGC others(10): Show |
T | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26+112_26+128delCC others(15): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421541 | |||||||
| chr17:55421622 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+48T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421622 | |||||||
| chr17:55421629 | T | C | 43 | a0001c0001t0001g0051 a0001c0001t0001g0219 a0001c0001t0002g0004 others(40): Show |
76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+41A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421629 |