Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55090 |
| ensemblid | ENSG00000141026.6 |
| hgncid | 25487 |
| symbol | MED9 |
| name | mediator complex subunit 9 |
| refseq_nuc | NM_018019.3 |
| refseq_prot | NP_060489.1 |
| ensembl_nuc | ENST00000268711.4 |
| ensembl_prot | ENSP00000268711.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 17477000 |
| end | 17493221 |
| strand | + |
| ver | v1.2 |
| region | chr17:17477000-17493221 |
| region5000 | chr17:17472000-17498221 |
| regionname0 | MED9_chr17_17477000_17493221 |
| regionname5000 | MED9_chr17_17472000_17498221 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 146 | 393 | 87 | 74 | 177 | 16 | 37 | 141 | MED9_chr17_17472000_17498221 | MED9 | MASAG others(141): Show |
chr17 | 17472000 | 17498221 |
| a0002 | 0/0 | 146 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | MASAG others(141): Show |
chr17 | 17472000 | 17498221 |
| a0003 | 0/0 | 146 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | MASAG others(141): Show |
chr17 | 17472000 | 17498221 |
| a0004 | 0/0 | 135 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | MASAG others(130): Show |
chr17 | 17472000 | 17498221 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 438 | 328 | 84 | 57 | 146 | 8 | 31 | MED9_chr17_17472000_17498221 | MED9 | ATGGC others(433): Show |
chr17 | 17472000 | 17498221 | ||
| a0001c0002 | 0/0 | 438 | 65 | 3 | 17 | 31 | 8 | 6 | MED9_chr17_17472000_17498221 | MED9 | ATGGC others(433): Show |
chr17 | 17472000 | 17498221 | ||
| a0002c0003 | 0/0 | 438 | 9 | 9 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | ATGGC others(433): Show |
chr17 | 17472000 | 17498221 | ||
| a0003c0005 | 0/0 | 438 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | ATGGC others(433): Show |
chr17 | 17472000 | 17498221 | ||
| a0004c0004 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | ATGGC others(402): Show |
chr17 | 17472000 | 17498221 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2209 | 289 | 62 | 52 | 140 | 7 | 26 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0002 | 0/0 | 2209 | 9 | 3 | 0 | 0 | 1 | 5 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0004 | 0/0 | 2205 | 6 | 6 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2200): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0006 | 0/0 | 2209 | 4 | 4 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0008 | 0/0 | 2209 | 3 | 0 | 0 | 3 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0009 | 0/0 | 2209 | 2 | 1 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0010 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2208): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0011 | 0/0 | 2209 | 2 | 0 | 2 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0012 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2208): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0013 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0015 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0016 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0017 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0018 | 0/0 | 2209 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0019 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0020 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0021 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0001t0022 | 0/0 | 2209 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0002t0001 | 0/0 | 2209 | 49 | 3 | 17 | 20 | 5 | 4 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0002t0003 | 0/0 | 2209 | 11 | 0 | 0 | 11 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0002t0007 | 0/0 | 2209 | 4 | 0 | 0 | 0 | 3 | 1 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0001c0002t0014 | 0/0 | 2209 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0002c0003t0001 | 0/0 | 2209 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0002c0003t0002 | 0/0 | 2209 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0002c0003t0005 | 0/0 | 2209 | 5 | 5 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0003c0005t0001 | 0/0 | 2209 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2204): Show |
chr17 | 17472000 | 17498221 |
| a0004c0004t0001 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | GCTTT others(2173): Show |
chr17 | 17472000 | 17498221 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 42 | 2 | 17 | 12 | 2 | 8 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0002 | 0/0 | 64 | 2 | 12 | 42 | 1 | 7 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0003 | 0/0 | 40 | 7 | 4 | 26 | 1 | 2 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0004 | 1/0 | 22 | 0 | 2 | 18 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0005 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0007 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 1 | 1 | 2 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0002g0008 | 0/0 | 7 | 1 | 0 | 0 | 1 | 5 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0004g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0009g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0011g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0018g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0019g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0021g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0001 | 0/0 | 32 | 0 | 13 | 13 | 2 | 4 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0003g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0007g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0001c0002t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0002c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0003c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| a0004c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | FIN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00323 | hp1 | a0001 | c0002 | t0007 | g0073 | EUR | FIN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0070 | EUR | FIN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0023 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01516 | hp1 | a0001 | c0002 | t0007 | g0028 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01517 | hp1 | a0001 | c0002 | t0007 | g0028 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01928 | hp1 | a0001 | c0001 | t0022 | g0002 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02055 | hp1 | a0001 | c0001 | t0021 | g0038 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02258 | hp2 | a0002 | c0003 | t0005 | g0017 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02293 | hp2 | a0001 | c0001 | t0018 | g0020 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02572 | hp1 | a0002 | c0003 | t0005 | g0017 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0079 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02683 | hp2 | a0001 | c0002 | t0007 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0046 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0088 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0075 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0017 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03041 | hp1 | a0002 | c0003 | t0005 | g0040 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0030 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03098 | hp2 | a0002 | c0003 | t0002 | g0030 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03540 | hp2 | a0002 | c0003 | t0005 | g0100 | AFR | GWD | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03831 | hp2 | a0001 | c0002 | t0014 | g0001 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04184 | hp1 | a0003 | c0005 | t0001 | g0056 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0068 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18971 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18982 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18997 | hp2 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19000 | hp2 | a0004 | c0004 | t0001 | g0077 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19062 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | YRI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | GIH | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0069 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | MED9_chr17_17472000_17498221 | MED9 | chr17 | 17472000 | 17498221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17477204 | G | T | 1 | a0002 | 9 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(6): Show |
missense_variant | MODERATE | c.163G>T | p.Ala55Ser | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/2 | 205/2209 | 163/441 | 55/146 | chr17 | 17477204 | |||
| chr17:17491373 | A | G | 1 | a0003 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.319A>G | p.Ile107Val | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 361/2209 | 319/441 | 107/146 | chr17 | 17491373 | |||
| chr17:17491439 | AATGAGCT others(24): Show |
A | 1 | a0004 | 1 | NA19000.hp2 | frameshift_variant | HIGH | c.386_416delATGAGCTT others(23): Show |
p.Asn129fs | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 428/2209 | 386/441 | 129/146 | chr17 | 17491439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17491297 | G | A | 1 | a0001c0002 | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
synonymous_variant | LOW | c.243G>A | p.Pro81Pro | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 285/2209 | 243/441 | 81/146 | chr17 | 17491297 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17477013 | C | T | 1 | a0001c0001t0008 | 3 | NA18944.hp2 NA18997.hp2 NA19081.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/2 | chr17 | 17477013 | |||||||
| chr17:17477035 | C | T | 1 | a0001c0001t0012 | 2 | HG02896.hp1 HG02897.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/2 | chr17 | 17477035 | |||||||
| chr17:17491520 | A | G | 1 | a0001c0001t0022 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 25 | chr17 | 17491520 | ||||||
| chr17:17491601 | T | A | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(2): Show |
21 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 106 | chr17 | 17491601 | ||||||
| chr17:17491603 | G | A | 1 | a0001c0001t0013 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 108 | chr17 | 17491603 | ||||||
| chr17:17491623 | C | T | 1 | a0001c0001t0021 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 128 | chr17 | 17491623 | ||||||
| chr17:17491651 | G | C | 1 | a0001c0001t0006 | 4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*156G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 156 | chr17 | 17491651 | ||||||
| chr17:17492018 | G | A | 1 | a0001c0002t0014 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*523G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 523 | chr17 | 17492018 | ||||||
| chr17:17492185 | T | C | 1 | a0001c0001t0015 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 690 | chr17 | 17492185 | ||||||
| chr17:17492215 | C | T | 1 | a0002c0003t0005 | 5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 720 | chr17 | 17492215 | ||||||
| chr17:17492337 | T | C | 1 | a0001c0001t0009 | 2 | HG01109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*842T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 842 | chr17 | 17492337 | ||||||
| chr17:17492344 | A | G | 1 | a0001c0001t0009 | 2 | HG01109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*849A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 849 | chr17 | 17492344 | ||||||
| chr17:17492411 | G | C | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 916 | chr17 | 17492411 | ||||||
| chr17:17492451 | TGAGA | T | 1 | a0001c0001t0004 | 6 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*962_*965delAGAG | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 962 | INFO_REALIGN_3_PRIME | chr17 | 17492451 | |||||
| chr17:17492472 | G | GGCCA | 2 | a0001c0001t0010 a0001c0001t0012 |
4 | HG02451.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*979_*982dupCCAG | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 983 | INFO_REALIGN_3_PRIME | chr17 | 17492472 | |||||
| chr17:17492499 | A | G | 1 | a0001c0002t0003 | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1004A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1004 | chr17 | 17492499 | ||||||
| chr17:17492514 | T | C | 1 | a0001c0001t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1019 | chr17 | 17492514 | ||||||
| chr17:17492763 | C | T | 1 | a0002c0003t0005 | 5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1268C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1268 | chr17 | 17492763 | ||||||
| chr17:17492815 | A | G | 1 | a0002c0003t0005 | 5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1320A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1320 | chr17 | 17492815 | ||||||
| chr17:17493006 | T | C | 1 | a0001c0002t0007 | 4 | HG00323.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1511T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1511 | chr17 | 17493006 | ||||||
| chr17:17493130 | G | T | 1 | a0001c0001t0020 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1635G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1635 | chr17 | 17493130 | ||||||
| chr17:17493150 | T | C | 1 | a0001c0001t0011 | 2 | HG00642.hp1 HG00735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1655T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1655 | chr17 | 17493150 | ||||||
| chr17:17493166 | C | T | 1 | a0001c0001t0019 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1671 | chr17 | 17493166 | ||||||
| chr17:17493191 | T | G | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1696T>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1696 | chr17 | 17493191 | ||||||
| chr17:17493204 | T | C | 2 | a0001c0001t0006 a0001c0001t0018 |
5 | HG02293.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1709T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 2/2 | 1709 | chr17 | 17493204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17477363 | C | A | 2 | a0002c0003t0005g0017 a0002c0003t0005g0040 |
4 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+98C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17477363 | |||||||
| chr17:17477573 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0102 |
4 | HG02486.hp1 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+308C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17477573 | |||||||
| chr17:17477680 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0101 |
7 | HG02109.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+415C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17477680 | |||||||
| chr17:17477742 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.224+477T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17477742 | |||||||
| chr17:17477898 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.224+633T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17477898 | |||||||
| chr17:17478248 | C | T | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+983C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478248 | |||||||
| chr17:17478332 | G | A | 1 | a0001c0002t0001g0043 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.224+1067G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478332 | |||||||
| chr17:17478450 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.224+1185T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478450 | |||||||
| chr17:17478829 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.224+1564C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478829 | |||||||
| chr17:17478857 | CA | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0076 others(2): Show |
11 | HG02109.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.224+1607delA | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17478857 | ||||||
| chr17:17478887 | A | G | 1 | a0001c0001t0001g0016 | 4 | NA18975.hp1 NA19007.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+1622A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478887 | |||||||
| chr17:17478931 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.224+1666T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17478931 | |||||||
| chr17:17479024 | A | G | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+1759A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479024 | |||||||
| chr17:17479266 | ATCT | A | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+2006_224+2008d others(5): Show |
MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17479266 | ||||||
| chr17:17479323 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224+2058C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479323 | |||||||
| chr17:17479519 | T | TA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.224+2268dupA | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17479519 | ||||||
| chr17:17479519 | T | TAA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(10): Show |
29 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.224+2267_224+2268d others(4): Show |
MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17479519 | ||||||
| chr17:17479528 | A | AG | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+2263_224+2264i others(3): Show |
MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479528 | |||||||
| chr17:17479601 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0034 |
14 | HG00673.hp1 HG02015.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.224+2336G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479601 | |||||||
| chr17:17479689 | A | C | 3 | a0001c0002t0001g0031 a0001c0002t0001g0070 a0001c0002t0001g0071 |
4 | HG00280.hp1 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+2424A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479689 | |||||||
| chr17:17479711 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA18971.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.224+2446C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479711 | |||||||
| chr17:17479782 | G | A | 1 | a0001c0001t0019g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.224+2517G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479782 | |||||||
| chr17:17479882 | A | G | 3 | a0002c0003t0001g0068 a0002c0003t0001g0069 a0002c0003t0002g0030 |
4 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+2617A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479882 | |||||||
| chr17:17479901 | G | T | 3 | a0002c0003t0001g0068 a0002c0003t0001g0069 a0002c0003t0002g0030 |
4 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+2636G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17479901 | |||||||
| chr17:17480001 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.224+2736G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480001 | |||||||
| chr17:17480110 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.224+2845C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480110 | |||||||
| chr17:17480265 | C | A | 1 | a0001c0001t0010g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.224+3000C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480265 | |||||||
| chr17:17480268 | C | G | 1 | a0001c0002t0001g0067 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.224+3003C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480268 | |||||||
| chr17:17480450 | G | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.224+3185G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480450 | |||||||
| chr17:17480518 | G | A | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+3253G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480518 | |||||||
| chr17:17480559 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0051 |
7 | HG01891.hp1 HG02257.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+3294G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480559 | |||||||
| chr17:17480595 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224+3330A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480595 | |||||||
| chr17:17480597 | G | A | 1 | a0002c0003t0002g0030 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.224+3332G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480597 | |||||||
| chr17:17480745 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.224+3480G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480745 | |||||||
| chr17:17480772 | G | A | 1 | a0002c0003t0005g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.224+3507G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480772 | |||||||
| chr17:17480827 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224+3562C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480827 | |||||||
| chr17:17480845 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.224+3580G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480845 | |||||||
| chr17:17480893 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.224+3628C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17480893 | |||||||
| chr17:17481163 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.224+3898C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481163 | |||||||
| chr17:17481186 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.224+3921A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481186 | |||||||
| chr17:17481237 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.224+3972G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481237 | |||||||
| chr17:17481315 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0054 |
7 | HG01081.hp1 HG01123.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+4050G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481315 | |||||||
| chr17:17481455 | G | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.224+4190G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481455 | |||||||
| chr17:17481571 | G | A | 1 | a0004c0004t0001g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.224+4306G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481571 | |||||||
| chr17:17481688 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(14): Show |
36 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.224+4423T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481688 | |||||||
| chr17:17481782 | A | C | 2 | a0002c0003t0005g0017 a0002c0003t0005g0040 |
4 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+4517A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481782 | |||||||
| chr17:17481876 | C | T | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+4611C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481876 | |||||||
| chr17:17481893 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.224+4628C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17481893 | |||||||
| chr17:17482098 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.224+4833G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482098 | |||||||
| chr17:17482109 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.224+4844T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482109 | |||||||
| chr17:17482219 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.224+4954A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482219 | |||||||
| chr17:17482387 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0018g0020 |
3 | HG01496.hp1 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.224+5122G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482387 | |||||||
| chr17:17482391 | T | C | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+5126T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482391 | |||||||
| chr17:17482518 | T | C | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+5253T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482518 | |||||||
| chr17:17482559 | TC | T | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+5295delC | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482559 | |||||||
| chr17:17482651 | T | G | 1 | a0001c0001t0009g0023 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.224+5386T>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482651 | |||||||
| chr17:17482660 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.224+5395C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482660 | |||||||
| chr17:17482676 | C | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.224+5411C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482676 | |||||||
| chr17:17482752 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.224+5487C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482752 | |||||||
| chr17:17482864 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.224+5599C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482864 | |||||||
| chr17:17482964 | T | TTCATGGT others(8): Show |
1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.224+5701_224+5715d others(17): Show |
MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17482964 | ||||||
| chr17:17482972 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.224+5707A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17482972 | |||||||
| chr17:17483081 | T | G | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+5816T>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483081 | |||||||
| chr17:17483183 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0096 a0001c0001t0021g0038 |
3 | HG02055.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.224+5918A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483183 | |||||||
| chr17:17483198 | AT | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0072 |
4 | HG02572.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+5936delT | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17483198 | ||||||
| chr17:17483511 | C | A | 1 | a0001c0001t0008g0084 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.224+6246C>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483511 | |||||||
| chr17:17483512 | A | C | 1 | a0001c0001t0008g0084 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.224+6247A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483512 | |||||||
| chr17:17483571 | C | G | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+6306C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483571 | |||||||
| chr17:17483667 | G | A | 1 | a0003c0005t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.224+6402G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483667 | |||||||
| chr17:17483679 | C | T | 1 | a0002c0003t0005g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.224+6414C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483679 | |||||||
| chr17:17483720 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.224+6455C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483720 | |||||||
| chr17:17483765 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.224+6500T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483765 | |||||||
| chr17:17483766 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.224+6501G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483766 | |||||||
| chr17:17483886 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224+6621A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483886 | |||||||
| chr17:17483887 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.224+6622C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17483887 | |||||||
| chr17:17484305 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225-6974G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484305 | |||||||
| chr17:17484359 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.225-6920C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484359 | |||||||
| chr17:17484527 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.225-6752C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484527 | |||||||
| chr17:17484585 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.225-6694C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484585 | |||||||
| chr17:17484600 | C | G | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225-6679C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484600 | |||||||
| chr17:17484611 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225-6668C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484611 | |||||||
| chr17:17484764 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.225-6515T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484764 | |||||||
| chr17:17484853 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-6426C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484853 | |||||||
| chr17:17484868 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(10): Show |
30 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.225-6411C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484868 | |||||||
| chr17:17484902 | G | C | 1 | a0001c0002t0001g0026 | 2 | NA18954.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.225-6377G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17484902 | |||||||
| chr17:17485105 | C | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.225-6174C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485105 | |||||||
| chr17:17485279 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.225-6000A>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485279 | |||||||
| chr17:17485280 | T | A | 1 | a0001c0001t0001g0015 | 4 | HG00735.hp2 HG01358.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-5999T>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485280 | |||||||
| chr17:17485378 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0054 |
2 | HG01081.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.225-5901C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485378 | |||||||
| chr17:17485412 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.225-5867G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485412 | |||||||
| chr17:17485546 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.225-5733A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485546 | |||||||
| chr17:17485577 | G | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.225-5702G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485577 | |||||||
| chr17:17485609 | G | C | 1 | a0001c0001t0008g0084 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.225-5670G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485609 | |||||||
| chr17:17485625 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0072 a0001c0001t0002g0045 others(1): Show |
6 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-5654C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485625 | |||||||
| chr17:17485839 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG02257.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-5440T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17485839 | |||||||
| chr17:17485937 | CAT | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0072 |
4 | HG02572.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-5340_225-5339d others(4): Show |
MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17485937 | ||||||
| chr17:17486058 | G | GT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(43): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.225-5211dupT | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17486058 | ||||||
| chr17:17486248 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.225-5031G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486248 | |||||||
| chr17:17486473 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.225-4806T>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486473 | |||||||
| chr17:17486590 | C | T | 3 | a0002c0003t0005g0017 a0002c0003t0005g0040 a0002c0003t0005g0100 |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-4689C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486590 | |||||||
| chr17:17486592 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(11): Show |
30 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.225-4687C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486592 | |||||||
| chr17:17486617 | G | A | 1 | a0001c0001t0009g0023 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.225-4662G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486617 | |||||||
| chr17:17486656 | G | A | 1 | a0001c0001t0001g0005 | 10 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.225-4623G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486656 | |||||||
| chr17:17486779 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.225-4500C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17486779 | |||||||
| chr17:17487103 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0021 |
7 | HG01192.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-4176G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487103 | |||||||
| chr17:17487173 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.225-4106T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487173 | |||||||
| chr17:17487202 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-4077A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487202 | |||||||
| chr17:17487257 | G | A | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-4022G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487257 | |||||||
| chr17:17487273 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.225-4006A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487273 | |||||||
| chr17:17487275 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.225-4004A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487275 | |||||||
| chr17:17487352 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-3927C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487352 | |||||||
| chr17:17487367 | T | C | 1 | a0002c0003t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.225-3912T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487367 | |||||||
| chr17:17487436 | T | C | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-3843T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487436 | |||||||
| chr17:17487464 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.225-3815G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487464 | |||||||
| chr17:17487650 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.225-3629C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487650 | |||||||
| chr17:17487785 | G | A | 1 | a0002c0003t0005g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-3494G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487785 | |||||||
| chr17:17487952 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.225-3327A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17487952 | |||||||
| chr17:17488057 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.225-3222C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488057 | |||||||
| chr17:17488086 | A | T | 1 | a0001c0001t0001g0014 | 4 | HG02486.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-3193A>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488086 | |||||||
| chr17:17488129 | C | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.225-3150C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488129 | |||||||
| chr17:17488204 | G | A | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-3075G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488204 | |||||||
| chr17:17488319 | G | T | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-2960G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488319 | |||||||
| chr17:17488458 | G | A | 1 | a0001c0001t0001g0019 | 3 | NA18951.hp2 NA18980.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.225-2821G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488458 | |||||||
| chr17:17488510 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-2769C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488510 | |||||||
| chr17:17488650 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.225-2629G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488650 | |||||||
| chr17:17488702 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0002g0045 |
2 | HG02647.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.225-2577G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488702 | |||||||
| chr17:17488831 | CA | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-2436delA | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr17 | 17488831 | ||||||
| chr17:17488841 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-2438A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488841 | |||||||
| chr17:17488958 | T | A | 1 | a0001c0001t0009g0023 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.225-2321T>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17488958 | |||||||
| chr17:17489222 | G | A | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-2057G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489222 | |||||||
| chr17:17489549 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.225-1730C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489549 | |||||||
| chr17:17489588 | A | G | 1 | a0001c0001t0009g0023 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.225-1691A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489588 | |||||||
| chr17:17489648 | G | A | 3 | a0002c0003t0001g0068 a0002c0003t0001g0069 a0002c0003t0002g0030 |
4 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-1631G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489648 | |||||||
| chr17:17489715 | C | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0002t0001g0013 |
5 | HG02074.hp2 NA18953.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-1564C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489715 | |||||||
| chr17:17489743 | C | G | 1 | a0001c0001t0004g0010 | 5 | HG01891.hp2 HG02145.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-1536C>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489743 | |||||||
| chr17:17489797 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0096 others(2): Show |
10 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-1482A>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489797 | |||||||
| chr17:17489806 | A | G | 1 | a0001c0001t0009g0023 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.225-1473A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489806 | |||||||
| chr17:17489882 | C | T | 1 | a0001c0001t0006g0033 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.225-1397C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489882 | |||||||
| chr17:17489922 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.225-1357G>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489922 | |||||||
| chr17:17489988 | C | T | 1 | a0001c0002t0001g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.225-1291C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17489988 | |||||||
| chr17:17490049 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.225-1230A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490049 | |||||||
| chr17:17490132 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0018g0020 |
3 | HG01496.hp1 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.225-1147A>G | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490132 | |||||||
| chr17:17490207 | A | T | 1 | a0001c0002t0007g0028 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.225-1072A>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490207 | |||||||
| chr17:17490367 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
19 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.225-912G>A | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490367 | |||||||
| chr17:17490453 | A | C | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-826A>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490453 | |||||||
| chr17:17490480 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.225-799T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490480 | |||||||
| chr17:17490487 | G | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0047 others(12): Show |
32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-792G>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490487 | |||||||
| chr17:17490538 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG00558.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.225-741T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490538 | |||||||
| chr17:17490811 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18986.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.225-468C>T | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17490811 | |||||||
| chr17:17491153 | T | C | 3 | a0002c0003t0001g0068 a0002c0003t0001g0069 a0002c0003t0002g0030 |
4 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-126T>C | MED9 | ENSG00000141026.6 | transcript | ENST00000268711.4 | protein_coding | 1/1 | chr17 | 17491153 |