Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80008 |
| ensemblid | ENSG00000121895.8 |
| hgncid | 26260 |
| symbol | TMEM156 |
| name | transmembrane protein 156 |
| refseq_nuc | NM_024943.3 |
| refseq_prot | NP_079219.1 |
| ensembl_nuc | ENST00000381938.4 |
| ensembl_prot | ENSP00000371364.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 38966744 |
| end | 39032409 |
| strand | - |
| ver | v1.2 |
| region | chr4:38966744-39032409 |
| region5000 | chr4:38961744-39037409 |
| regionname0 | TMEM156_chr4_38966744_39032409 |
| regionname5000 | TMEM156_chr4_38961744_39037409 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 296 | 253 | 68 | 55 | 98 | 5 | 25 | 68 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| a0002 | 0/0 | 296 | 112 | 13 | 15 | 64 | 2 | 18 | 54 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| a0003 | 0/0 | 296 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| a0004 | 0/0 | 296 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| a0005 | 0/0 | 296 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| a0006 | 0/0 | 296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | MTKTA others(291): Show |
chr4 | 38961744 | 39037409 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 888 | 233 | 67 | 44 | 92 | 4 | 25 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0001c0003 | 1/0 | 888 | 18 | 0 | 10 | 6 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0001c0008 | 0/0 | 888 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0001c0009 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0002c0002 | 0/0 | 888 | 112 | 13 | 15 | 64 | 2 | 18 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0003c0004 | 0/0 | 888 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0004c0005 | 0/0 | 888 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0005c0006 | 0/0 | 888 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 | ||
| a0006c0007 | 0/0 | 888 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | ATGAC others(883): Show |
chr4 | 38961744 | 39037409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1923 | 98 | 21 | 24 | 38 | 3 | 12 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0002 | 0/0 | 1923 | 46 | 16 | 8 | 17 | 0 | 5 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0003 | 0/0 | 1924 | 27 | 4 | 8 | 11 | 0 | 4 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0004 | 0/0 | 1922 | 28 | 3 | 2 | 18 | 1 | 4 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1917): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0005 | 0/0 | 1926 | 17 | 15 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1921): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0006 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0007 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0008 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0009 | 0/0 | 1924 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0010 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0011 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0012 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0013 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0014 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0015 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0016 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0017 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1917): Show |
chr4 | 38961744 | 39037409 |
| a0001c0001t0018 | 0/1 | 1923 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0003t0001 | 1/0 | 1923 | 5 | 0 | 2 | 1 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0003t0002 | 0/0 | 1923 | 7 | 0 | 5 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0001c0003t0003 | 0/0 | 1924 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0003t0004 | 0/0 | 1922 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1917): Show |
chr4 | 38961744 | 39037409 |
| a0001c0003t0006 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0008t0003 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0001c0009t0001 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0001 | 0/0 | 1923 | 47 | 4 | 7 | 22 | 2 | 12 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0002 | 0/0 | 1923 | 30 | 4 | 5 | 20 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0003 | 0/0 | 1924 | 16 | 1 | 3 | 11 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0004 | 0/0 | 1922 | 12 | 2 | 0 | 7 | 0 | 3 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1917): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0005 | 0/0 | 1926 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1921): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0006 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0007 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0002c0002t0011 | 0/0 | 1923 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0003c0004t0001 | 0/0 | 1923 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0003c0004t0002 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0003c0004t0003 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0004c0005t0001 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0004c0005t0002 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0004c0005t0003 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0004c0005t0005 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1921): Show |
chr4 | 38961744 | 39037409 |
| a0005c0006t0001 | 0/0 | 1923 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0005c0006t0003 | 0/0 | 1924 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0006c0007t0001 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1918): Show |
chr4 | 38961744 | 39037409 |
| a0006c0007t0003 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| a0006c0007t0006 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | GCATT others(1919): Show |
chr4 | 38961744 | 39037409 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0009g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0013g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0014g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0015g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0016g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0017g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0018g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0362 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0006g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0008t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0009t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0005g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0011g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0007t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0007t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0007t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0071 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0084 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00280 | hp1 | a0005 | c0006 | t0001 | g0055 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0186 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0335 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0360 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0382 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0287 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0213 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0183 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0352 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0351 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0218 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0367 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0353 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01074 | hp2 | a0005 | c0006 | t0001 | g0029 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0379 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0187 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0190 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01255 | hp2 | a0001 | c0008 | t0003 | g0005 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0238 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0349 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0363 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0302 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0136 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01981 | hp1 | a0001 | c0003 | t0006 | g0348 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0098 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0132 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0200 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0221 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02071 | hp2 | a0003 | c0004 | t0002 | g0144 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0148 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0365 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CDX | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0160 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02300 | hp2 | a0002 | c0002 | t0003 | g0052 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02451 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02622 | hp1 | a0004 | c0005 | t0005 | g0249 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0371 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02647 | hp2 | a0006 | c0007 | t0003 | g0288 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02738 | hp1 | a0005 | c0006 | t0003 | g0134 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0233 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02818 | hp1 | a0002 | c0002 | t0004 | g0043 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02818 | hp2 | a0006 | c0007 | t0001 | g0369 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0378 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02895 | hp2 | a0001 | c0001 | t0013 | g0266 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0375 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0300 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0085 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02976 | hp1 | a0004 | c0005 | t0003 | g0201 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0372 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0167 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03139 | hp2 | a0004 | c0005 | t0002 | g0254 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03195 | hp1 | a0002 | c0002 | t0005 | g0380 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03225 | hp2 | a0006 | c0007 | t0006 | g0289 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0376 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03516 | hp1 | a0001 | c0009 | t0001 | g0176 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0259 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0370 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0227 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0226 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0050 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0286 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04184 | hp2 | a0002 | c0002 | t0011 | g0230 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18612 | hp1 | a0001 | c0001 | t0017 | g0099 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0305 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18747 | hp2 | a0003 | c0004 | t0002 | g0125 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18940 | hp1 | a0001 | c0003 | t0004 | g0020 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18940 | hp2 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0234 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0205 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0097 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18948 | hp2 | a0001 | c0001 | t0016 | g0118 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0127 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0138 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0357 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0377 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0126 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18974 | hp1 | a0002 | c0002 | t0006 | g0014 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0340 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0355 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18986 | hp2 | a0001 | c0003 | t0004 | g0334 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0204 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18997 | hp2 | a0002 | c0002 | t0003 | g0381 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0089 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0294 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19009 | hp2 | a0002 | c0002 | t0007 | g0308 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19030 | hp2 | a0004 | c0005 | t0001 | g0133 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19058 | hp2 | a0002 | c0002 | t0004 | g0235 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19063 | hp1 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19063 | hp2 | a0002 | c0002 | t0007 | g0310 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0356 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19072 | hp1 | a0002 | c0002 | t0004 | g0113 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19082 | hp1 | a0003 | c0004 | t0002 | g0123 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19083 | hp2 | a0002 | c0002 | t0006 | g0065 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19087 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0258 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0280 | SAS | GIH | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01123 | hp2 | a0005 | c0006 | t0001 | g0220 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0006 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | USA | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | USA | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0373 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0267 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0156 | REF | REF | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0362 | REF | REF | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38971071 | T | C | 2 | a0001 a0002 |
5 | HG02080.hp1 HG04184.hp2 NA19009.hp2 others(2): Show |
stop_retained_variant | LOW | c.890A>G | p.Ter297Ter | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/7 | 986/1923 | 890/891 | 297/296 | chr4 | 38971071 | |||
| chr4:38986345 | C | T | 1 | a0005 | 4 | HG00280.hp1 HG01074.hp2 HG01123.hp2 others(1): Show |
missense_variant | MODERATE | c.814G>A | p.Val272Ile | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/7 | 910/1923 | 814/891 | 272/296 | chr4 | 38986345 | |||
| chr4:38988955 | A | G | 1 | a0003 | 8 | HG02071.hp2 NA18747.hp2 NA18944.hp1 others(5): Show |
missense_variant | MODERATE | c.635T>C | p.Met212Thr | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/7 | 731/1923 | 635/891 | 212/296 | chr4 | 38988955 | |||
| chr4:38993781 | A | T | 1 | a0006 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.576T>A | p.Asn192Lys | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/7 | 672/1923 | 576/891 | 192/296 | chr4 | 38993781 | |||
| chr4:38998685 | A | G | 2 | a0002 a0003 |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
missense_variant | MODERATE | c.313T>C | p.Ser105Pro | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/7 | 409/1923 | 313/891 | 105/296 | chr4 | 38998685 | |||
| chr4:38998855 | T | C | 1 | a0004 | 6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.143A>G | p.Tyr48Cys | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/7 | 239/1923 | 143/891 | 48/296 | chr4 | 38998855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38971127 | C | T | 1 | a0001c0009 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.834G>A | p.Thr278Thr | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/7 | 930/1923 | 834/891 | 278/296 | chr4 | 38971127 | |||
| chr4:38993754 | T | C | 8 | a0001c0001 a0001c0008 a0001c0009 others(5): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.603A>G | p.Leu201Leu | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/7 | 699/1923 | 603/891 | 201/296 | chr4 | 38993754 | |||
| chr4:39032272 | C | T | 1 | a0001c0008 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.42G>A | p.Val14Val | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/7 | 138/1923 | 42/891 | 14/296 | chr4 | 39032272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38966782 | G | A | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4288 | chr4 | 38966782 | ||||||
| chr4:38966800 | A | AT | 17 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(14): Show |
64 | HG00438.hp1 HG00673.hp1 HG00733.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*879dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4269 | chr4 | 38966800 | ||||||
| chr4:38966800 | AT | A | 4 | a0001c0001t0004 a0001c0001t0017 a0001c0003t0004 others(1): Show |
43 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*879delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4269 | chr4 | 38966800 | ||||||
| chr4:38966821 | T | TTTG | 3 | a0001c0001t0005 a0002c0002t0005 a0004c0005t0005 |
20 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*858_*859insCAA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4248 | chr4 | 38966821 | ||||||
| chr4:38966823 | A | T | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(8): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*857T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4247 | chr4 | 38966823 | ||||||
| chr4:38966829 | A | T | 1 | a0001c0001t0008 | 2 | HG02886.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*851T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4241 | chr4 | 38966829 | ||||||
| chr4:38966907 | T | G | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*773A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4163 | chr4 | 38966907 | ||||||
| chr4:38966965 | C | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4105 | chr4 | 38966965 | ||||||
| chr4:38967026 | C | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4044 | chr4 | 38967026 | ||||||
| chr4:38967045 | C | T | 1 | a0001c0001t0016 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4025 | chr4 | 38967045 | ||||||
| chr4:38967186 | C | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3884 | chr4 | 38967186 | ||||||
| chr4:38967280 | A | C | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3790 | chr4 | 38967280 | ||||||
| chr4:38967317 | A | G | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3753 | chr4 | 38967317 | ||||||
| chr4:38967355 | T | C | 1 | a0001c0001t0009 | 2 | HG01884.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*325A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3715 | chr4 | 38967355 | ||||||
| chr4:38967409 | T | G | 1 | a0001c0001t0015 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3661 | chr4 | 38967409 | ||||||
| chr4:38967411 | C | T | 1 | a0001c0001t0015 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3659 | chr4 | 38967411 | ||||||
| chr4:38967616 | C | T | 1 | a0001c0001t0014 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3454 | chr4 | 38967616 | ||||||
| chr4:38967618 | C | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3452 | chr4 | 38967618 | ||||||
| chr4:38967623 | C | T | 1 | a0001c0001t0012 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3447 | chr4 | 38967623 | ||||||
| chr4:38967633 | G | A | 1 | a0001c0001t0010 | 2 | HG03130.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*47C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3437 | chr4 | 38967633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38967753 | G | C | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-112C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967753 | |||||||
| chr4:38967806 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(78): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.*39-165C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967806 | |||||||
| chr4:38967973 | A | G | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-332T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967973 | |||||||
| chr4:38968078 | C | T | 2 | a0001c0001t0001g0247 a0004c0005t0001g0133 |
2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*39-437G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968078 | |||||||
| chr4:38968242 | C | T | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-601G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968242 | |||||||
| chr4:38968289 | G | T | 1 | a0002c0002t0007g0308 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.*39-648C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968289 | |||||||
| chr4:38968340 | G | A | 1 | a0002c0002t0001g0284 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*39-699C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968340 | |||||||
| chr4:38968350 | A | G | 1 | a0002c0002t0001g0330 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*39-709T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968350 | |||||||
| chr4:38968359 | G | A | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-718C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968359 | |||||||
| chr4:38968402 | A | C | 2 | a0001c0001t0013g0266 a0006c0007t0001g0369 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.*39-761T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968402 | |||||||
| chr4:38968488 | T | A | 1 | a0001c0001t0015g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-847A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968488 | |||||||
| chr4:38968499 | G | A | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-858C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968499 | |||||||
| chr4:38968535 | T | C | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-894A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968535 | |||||||
| chr4:38968550 | A | G | 1 | a0001c0001t0001g0354 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*39-909T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968550 | |||||||
| chr4:38968699 | A | G | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-1058T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968699 | |||||||
| chr4:38968813 | G | A | 1 | a0001c0001t0004g0344 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.*39-1172C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968813 | |||||||
| chr4:38968968 | G | A | 5 | a0001c0001t0004g0159 a0001c0001t0004g0170 a0001c0001t0004g0174 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39-1327C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968968 | |||||||
| chr4:38969086 | A | G | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-1445T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969086 | |||||||
| chr4:38969093 | G | C | 1 | a0001c0001t0015g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-1452C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969093 | |||||||
| chr4:38969094 | C | G | 1 | a0001c0001t0015g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-1453G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969094 | |||||||
| chr4:38969125 | G | C | 9 | a0001c0001t0004g0009 a0001c0001t0004g0103 a0001c0001t0004g0224 others(6): Show |
9 | HG00597.hp2 HG00621.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.*39-1484C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969125 | |||||||
| chr4:38969437 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0018 others(362): Show |
369 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.*38+1595T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969437 | |||||||
| chr4:38969448 | GCAC | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1581_*38+1583d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969448 | |||||||
| chr4:38969544 | T | C | 2 | a0001c0001t0002g0199 a0001c0001t0002g0261 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*38+1488A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969544 | |||||||
| chr4:38969545 | A | G | 2 | a0001c0001t0003g0214 a0002c0002t0001g0038 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.*38+1487T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969545 | |||||||
| chr4:38969558 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1474G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969558 | |||||||
| chr4:38969597 | T | C | 1 | a0002c0002t0004g0050 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*38+1435A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969597 | |||||||
| chr4:38969599 | G | A | 1 | a0006c0007t0003g0288 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*38+1433C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969599 | |||||||
| chr4:38969670 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1362C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969670 | |||||||
| chr4:38969700 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02818.hp2 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.*38+1332A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969700 | |||||||
| chr4:38969711 | G | A | 1 | a0001c0001t0005g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*38+1321C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969711 | |||||||
| chr4:38969762 | T | C | 103 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0182 others(100): Show |
104 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.*38+1270A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969762 | |||||||
| chr4:38969888 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1144G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969888 | |||||||
| chr4:38969908 | T | C | 1 | a0001c0003t0004g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.*38+1124A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969908 | |||||||
| chr4:38969988 | T | C | 9 | a0001c0001t0003g0173 a0001c0001t0003g0192 a0001c0001t0003g0265 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*38+1044A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969988 | |||||||
| chr4:38970146 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+886A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | |||||||
| chr4:38970146 | T | TTG | 110 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0182 others(107): Show |
111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.*38+884_*38+885dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | |||||||
| chr4:38970146 | T | TTGTG | 5 | a0001c0001t0002g0057 a0001c0001t0002g0199 a0002c0002t0002g0225 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.*38+882_*38+885dup others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | |||||||
| chr4:38970148 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+884C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970148 | |||||||
| chr4:38970179 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+853G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970179 | |||||||
| chr4:38970182 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*38+850C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970182 | |||||||
| chr4:38970221 | T | C | 1 | a0001c0001t0005g0379 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.*38+811A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970221 | |||||||
| chr4:38970264 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+768T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970264 | |||||||
| chr4:38970285 | T | TC | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+746_*38+747ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970285 | |||||||
| chr4:38970287 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+745C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970287 | |||||||
| chr4:38970381 | T | A | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*38+651A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970381 | |||||||
| chr4:38970652 | C | A | 21 | a0001c0001t0001g0041 a0001c0001t0001g0255 a0001c0001t0001g0263 others(18): Show |
21 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.*38+380G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970652 | |||||||
| chr4:38970754 | C | T | 11 | a0001c0001t0001g0196 a0001c0001t0001g0295 a0001c0001t0003g0173 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.*38+278G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970754 | |||||||
| chr4:38970781 | A | G | 1 | a0001c0001t0004g0331 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*38+251T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970781 | |||||||
| chr4:38970872 | G | A | 4 | a0001c0001t0002g0171 a0001c0001t0002g0373 a0004c0005t0002g0254 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.*38+160C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970872 | |||||||
| chr4:38971173 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-36T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971173 | |||||||
| chr4:38971200 | T | G | 1 | a0002c0002t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.824-63A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971200 | |||||||
| chr4:38971360 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-223C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971360 | |||||||
| chr4:38971475 | T | G | 1 | a0002c0002t0004g0006 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824-338A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971475 | |||||||
| chr4:38971795 | A | AT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-659dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971795 | |||||||
| chr4:38971812 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0018 others(280): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.824-675T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971812 | |||||||
| chr4:38971820 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-683C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971820 | |||||||
| chr4:38971977 | C | T | 2 | a0001c0001t0004g0009 a0002c0002t0004g0235 |
2 | NA19057.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.824-840G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971977 | |||||||
| chr4:38972145 | C | T | 2 | a0002c0002t0001g0282 a0002c0002t0001g0286 |
2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.824-1008G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972145 | |||||||
| chr4:38972211 | G | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0370 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.824-1074C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972211 | |||||||
| chr4:38972242 | A | AT | 12 | a0001c0001t0001g0015 a0001c0001t0001g0207 a0001c0001t0001g0272 others(9): Show |
12 | HG00423.hp1 HG01243.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1106dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.824-1116_824-1106d others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0322 others(1): Show |
4 | HG03942.hp1 NA18962.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1117_824-1106d others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | AT | A | 29 | a0001c0001t0001g0131 a0001c0001t0001g0169 a0001c0001t0001g0188 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.824-1106delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | ATT | A | 23 | a0001c0001t0001g0164 a0001c0001t0001g0255 a0001c0001t0001g0291 others(20): Show |
23 | HG00438.hp1 HG00621.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-1107_824-1106d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | ATTT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(115): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.824-1108_824-1106d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | ATTTT | A | 99 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0002g0016 others(96): Show |
100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.824-1109_824-1106d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972242 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0004g0159 a0001c0001t0004g0170 a0001c0001t0004g0174 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1115_824-1106d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | |||||||
| chr4:38972316 | C | T | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.824-1179G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972316 | |||||||
| chr4:38972348 | G | A | 1 | a0001c0003t0002g0007 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.824-1211C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972348 | |||||||
| chr4:38972447 | C | T | 1 | a0001c0001t0003g0337 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.824-1310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972447 | |||||||
| chr4:38972564 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.824-1427A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972564 | |||||||
| chr4:38972650 | C | CA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1514_824-1513i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972650 | |||||||
| chr4:38972658 | C | G | 1 | a0001c0001t0003g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-1521G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972658 | |||||||
| chr4:38972838 | A | C | 105 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0182 others(102): Show |
106 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.824-1701T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972838 | |||||||
| chr4:38972884 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(3): Show |
6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1747A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972884 | |||||||
| chr4:38973126 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-1989C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973126 | |||||||
| chr4:38973156 | T | C | 2 | a0001c0001t0004g0224 a0002c0002t0004g0138 |
2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.824-2019A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973156 | |||||||
| chr4:38973389 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2252A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973389 | |||||||
| chr4:38973433 | T | C | 5 | a0001c0001t0004g0159 a0001c0001t0004g0170 a0001c0001t0004g0174 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2296A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973433 | |||||||
| chr4:38973476 | A | G | 8 | a0001c0001t0002g0076 a0001c0001t0002g0326 a0001c0001t0006g0340 others(5): Show |
8 | HG00609.hp2 HG02083.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-2339T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973476 | |||||||
| chr4:38973482 | T | C | 1 | a0002c0002t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-2345A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973482 | |||||||
| chr4:38973526 | A | C | 1 | a0001c0001t0004g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.824-2389T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973526 | |||||||
| chr4:38973639 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2502G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973639 | |||||||
| chr4:38973677 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2540G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973677 | |||||||
| chr4:38973922 | A | G | 5 | a0001c0001t0004g0159 a0001c0001t0004g0170 a0001c0001t0004g0174 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2785T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973922 | |||||||
| chr4:38974058 | C | T | 3 | a0002c0002t0001g0111 a0002c0002t0001g0282 a0002c0002t0001g0286 |
3 | HG02735.hp2 HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.824-2921G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | |||||||
| chr4:38974058 | CGT | C | 53 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0109 others(50): Show |
53 | HG00099.hp1 HG01255.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.824-2923_824-2922d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | |||||||
| chr4:38974058 | CGTGT | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0090 others(8): Show |
11 | HG02129.hp1 HG02895.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.824-2925_824-2922d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | |||||||
| chr4:38974058 | CGTGTGT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.824-2927_824-2922d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | |||||||
| chr4:38974207 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.824-3071dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974207 | |||||||
| chr4:38974207 | CT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0196 others(27): Show |
30 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.824-3071delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974207 | |||||||
| chr4:38974209 | T | C | 9 | a0001c0001t0002g0028 a0001c0001t0002g0260 a0001c0001t0002g0301 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-3072A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974209 | |||||||
| chr4:38974519 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3382C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974519 | |||||||
| chr4:38974674 | A | AT | 41 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0131 others(38): Show |
41 | HG00099.hp1 HG01167.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.824-3538dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | |||||||
| chr4:38974674 | A | ATT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-3539_824-3538d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | |||||||
| chr4:38974674 | AT | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(107): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.824-3538delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | |||||||
| chr4:38974710 | C | T | 2 | a0001c0001t0001g0034 a0006c0007t0003g0288 |
2 | HG02647.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.824-3573G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974710 | |||||||
| chr4:38974874 | T | A | 1 | a0006c0007t0003g0288 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.824-3737A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974874 | |||||||
| chr4:38974898 | C | A | 1 | a0001c0001t0001g0354 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.824-3761G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974898 | |||||||
| chr4:38974913 | A | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0018 others(279): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.824-3776T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974913 | |||||||
| chr4:38974915 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3778G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974915 | |||||||
| chr4:38974950 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0292 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.824-3813C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974950 | |||||||
| chr4:38974963 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3826C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974963 | |||||||
| chr4:38975005 | G | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3868C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975005 | |||||||
| chr4:38975029 | C | T | 6 | a0001c0001t0001g0255 a0001c0001t0005g0172 a0001c0001t0005g0248 others(3): Show |
6 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-3892G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975029 | |||||||
| chr4:38975189 | T | C | 2 | a0001c0001t0001g0366 a0005c0006t0001g0220 |
2 | HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.824-4052A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975189 | |||||||
| chr4:38975223 | T | C | 1 | a0001c0001t0010g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-4086A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975223 | |||||||
| chr4:38975372 | CTTTTTTC others(6): Show |
C | 11 | a0001c0001t0001g0196 a0001c0001t0001g0295 a0001c0001t0003g0173 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.824-4248_824-4236d others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975372 | |||||||
| chr4:38975381 | TTTC | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-4247_824-4245d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975381 | |||||||
| chr4:38975383 | TC | T | 100 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0002g0016 others(97): Show |
101 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.824-4247delG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975383 | |||||||
| chr4:38975384 | C | T | 2 | a0002c0002t0002g0120 a0003c0004t0002g0125 |
2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.824-4247G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975384 | |||||||
| chr4:38975384 | CT | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.824-4248delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975384 | |||||||
| chr4:38975416 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0321 |
2 | HG01256.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.824-4279A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975416 | |||||||
| chr4:38975508 | G | A | 108 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0090 others(105): Show |
109 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.824-4371C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975508 | |||||||
| chr4:38975555 | A | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0090 others(108): Show |
112 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.824-4418T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975555 | |||||||
| chr4:38975617 | G | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0090 others(107): Show |
111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.824-4480C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975617 | |||||||
| chr4:38975722 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.824-4585T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975722 | |||||||
| chr4:38975744 | C | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0196 a0001c0001t0001g0263 others(24): Show |
27 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.824-4607G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975744 | |||||||
| chr4:38975746 | C | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0090 others(107): Show |
111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.824-4609G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975746 | |||||||
| chr4:38975908 | G | C | 4 | a0002c0002t0001g0145 a0002c0002t0001g0212 a0003c0004t0001g0127 others(1): Show |
4 | NA18951.hp1 NA18955.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-4771C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975908 | |||||||
| chr4:38975912 | G | A | 1 | a0002c0002t0002g0333 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.824-4775C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975912 | |||||||
| chr4:38975941 | A | G | 1 | a0001c0001t0004g0329 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.824-4804T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975941 | |||||||
| chr4:38976012 | C | A | 7 | a0001c0001t0001g0255 a0001c0001t0005g0172 a0001c0001t0005g0248 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-4875G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976012 | |||||||
| chr4:38976013 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0131 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG01255.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.824-4876C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976013 | |||||||
| chr4:38976084 | C | T | 16 | a0001c0001t0001g0042 a0001c0001t0001g0162 a0001c0001t0001g0169 others(13): Show |
16 | HG01255.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.824-4947G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976084 | |||||||
| chr4:38976275 | G | A | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.824-5138C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976275 | |||||||
| chr4:38976289 | C | CA | 10 | a0001c0001t0001g0135 a0001c0001t0001g0303 a0001c0001t0002g0189 others(7): Show |
10 | HG00597.hp1 HG01361.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-5153dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | |||||||
| chr4:38976289 | CA | C | 144 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0034 others(141): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.824-5153delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | |||||||
| chr4:38976289 | CAA | C | 92 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0322 others(89): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.824-5154_824-5153d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | |||||||
| chr4:38976289 | CAAA | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(17): Show |
21 | HG01109.hp2 HG02129.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.824-5155_824-5153d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | |||||||
| chr4:38976354 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(10): Show |
13 | HG01109.hp2 HG02129.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-5217C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976354 | |||||||
| chr4:38976357 | G | A | 103 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0002g0016 others(100): Show |
104 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.824-5220C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976357 | |||||||
| chr4:38976381 | A | T | 115 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0026 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.824-5244T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976381 | |||||||
| chr4:38976408 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0154 others(7): Show |
10 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.824-5271G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976408 | |||||||
| chr4:38976551 | C | T | 97 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0002g0016 others(94): Show |
98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.824-5414G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976551 | |||||||
| chr4:38976563 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0002c0002t0003g0215 |
3 | NA18941.hp1 NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.824-5426C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976563 | |||||||
| chr4:38976669 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0208 others(4): Show |
7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-5532T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976669 | |||||||
| chr4:38976807 | C | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0047 others(144): Show |
149 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.824-5670G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976807 | |||||||
| chr4:38976890 | T | TTTG | 168 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(165): Show |
170 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.824-5756_824-5754d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | |||||||
| chr4:38976890 | T | TTTGTTGT others(2): Show |
30 | a0001c0001t0001g0182 a0001c0001t0003g0242 a0001c0001t0004g0009 others(27): Show |
31 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-5762_824-5754d others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | |||||||
| chr4:38976890 | T | TTTGTTGT others(8): Show |
1 | a0001c0001t0004g0081 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.824-5768_824-5754d others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | |||||||
| chr4:38976890 | TTTG | T | 18 | a0001c0001t0001g0042 a0001c0001t0001g0131 a0001c0001t0001g0162 others(15): Show |
18 | HG00099.hp1 HG01255.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.824-5756_824-5754d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | |||||||
| chr4:38976890 | TTTGTTG | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0034 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.824-5759_824-5754d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | |||||||
| chr4:38976980 | A | T | 2 | a0001c0001t0008g0063 a0001c0001t0008g0244 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.824-5843T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976980 | |||||||
| chr4:38977066 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-5929C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977066 | |||||||
| chr4:38977072 | T | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0090 others(30): Show |
33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5935A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977072 | |||||||
| chr4:38977117 | C | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0090 others(29): Show |
32 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-5980G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977117 | |||||||
| chr4:38977125 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0090 others(30): Show |
33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5988T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977125 | |||||||
| chr4:38977126 | AACT | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0090 others(30): Show |
33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5992_824-5990d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977126 | |||||||
| chr4:38977130 | C | T | 33 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0090 others(30): Show |
33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5993G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977130 | |||||||
| chr4:38977148 | G | A | 6 | a0001c0001t0001g0255 a0001c0001t0005g0172 a0001c0001t0005g0248 others(3): Show |
6 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-6011C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977148 | |||||||
| chr4:38977208 | A | C | 1 | a0002c0002t0001g0236 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.824-6071T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977208 | |||||||
| chr4:38977293 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.824-6156C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977293 | |||||||
| chr4:38977359 | A | G | 1 | a0002c0002t0001g0216 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.824-6222T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977359 | |||||||
| chr4:38977433 | A | T | 41 | a0001c0001t0001g0182 a0001c0001t0003g0242 a0001c0001t0004g0009 others(38): Show |
42 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.824-6296T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977433 | |||||||
| chr4:38977492 | T | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0162 a0001c0001t0001g0169 others(4): Show |
7 | HG00099.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-6355A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977492 | |||||||
| chr4:38977524 | C | T | 3 | a0001c0001t0010g0167 a0001c0001t0013g0266 a0006c0007t0001g0369 |
3 | HG02818.hp2 HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.824-6387G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977524 | |||||||
| chr4:38977630 | A | G | 1 | a0001c0001t0010g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-6493T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977630 | |||||||
| chr4:38977786 | G | C | 1 | a0002c0002t0004g0128 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-6649C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977786 | |||||||
| chr4:38977841 | A | G | 3 | a0001c0001t0005g0060 a0001c0001t0005g0198 a0004c0005t0005g0249 |
3 | HG01243.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.824-6704T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977841 | |||||||
| chr4:38977937 | T | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(344): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.824-6800A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977937 | |||||||
| chr4:38977946 | C | T | 1 | a0002c0002t0001g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.824-6809G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977946 | |||||||
| chr4:38977987 | A | G | 139 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(138): Show |
intron_variant | MODIFIER | c.824-6850T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977987 | |||||||
| chr4:38978049 | A | G | 2 | a0001c0001t0001g0018 a0002c0002t0004g0227 |
2 | HG01361.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.824-6912T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978049 | |||||||
| chr4:38978062 | T | C | 32 | a0001c0001t0001g0041 a0001c0001t0001g0164 a0001c0001t0001g0196 others(29): Show |
32 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.824-6925A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978062 | |||||||
| chr4:38978191 | T | A | 42 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0086 others(39): Show |
42 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.824-7054A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978191 | |||||||
| chr4:38978258 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(123): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.824-7121T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978258 | |||||||
| chr4:38978267 | T | A | 1 | a0001c0001t0004g0048 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824-7130A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978267 | |||||||
| chr4:38978267 | T | TA | 96 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0041 others(93): Show |
96 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.824-7131dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978267 | |||||||
| chr4:38978305 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG02451.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-7168A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978305 | |||||||
| chr4:38978316 | C | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(363): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.824-7179G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978316 | |||||||
| chr4:38978376 | T | C | 3 | a0001c0001t0001g0315 a0001c0001t0004g0074 a0001c0001t0004g0142 |
3 | HG03704.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.824-7239A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978376 | |||||||
| chr4:38978387 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-7250G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978387 | |||||||
| chr4:38978444 | T | C | 250 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(247): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.824-7307A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978444 | |||||||
| chr4:38978503 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.824-7366G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978503 | |||||||
| chr4:38978521 | C | T | 152 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0037 others(149): Show |
153 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.824-7384G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978521 | |||||||
| chr4:38978566 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0291 a0001c0001t0004g0101 others(2): Show |
5 | HG02027.hp2 NA18957.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-7429G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978566 | |||||||
| chr4:38978721 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0181 |
2 | NA18961.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.824-7584T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978721 | |||||||
| chr4:38978749 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0010g0167 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.823+7587A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978749 | |||||||
| chr4:38978908 | G | A | 1 | a0001c0001t0004g0107 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.823+7428C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978908 | |||||||
| chr4:38979082 | A | G | 2 | a0003c0004t0001g0204 a0003c0004t0001g0205 |
2 | NA18944.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.823+7254T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979082 | |||||||
| chr4:38979307 | A | C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0196 a0001c0001t0001g0245 others(10): Show |
13 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+7029T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979307 | |||||||
| chr4:38979379 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0004g0179 |
2 | NA18961.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.823+6957C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979379 | |||||||
| chr4:38979451 | T | C | 1 | a0001c0001t0009g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.823+6885A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979451 | |||||||
| chr4:38979471 | T | C | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+6865A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979471 | |||||||
| chr4:38979646 | T | G | 1 | a0001c0001t0005g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823+6690A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979646 | |||||||
| chr4:38979683 | T | G | 1 | a0001c0001t0004g0222 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.823+6653A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979683 | |||||||
| chr4:38979775 | A | G | 1 | a0002c0002t0001g0217 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.823+6561T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979775 | |||||||
| chr4:38979806 | A | C | 1 | a0001c0001t0004g0317 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.823+6530T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979806 | |||||||
| chr4:38979821 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0015g0300 |
2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.823+6515T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979821 | |||||||
| chr4:38979822 | G | C | 58 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(55): Show |
58 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.823+6514C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979822 | |||||||
| chr4:38979865 | C | T | 4 | a0001c0001t0001g0257 a0001c0001t0002g0044 a0001c0001t0003g0192 others(1): Show |
4 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+6471G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979865 | |||||||
| chr4:38979990 | C | A | 1 | a0001c0001t0005g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+6346G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979990 | |||||||
| chr4:38980040 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.823+6296T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980040 | |||||||
| chr4:38980120 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+6216T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980120 | |||||||
| chr4:38980185 | T | TA | 25 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0102 others(22): Show |
25 | HG00423.hp1 HG01081.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.823+6150dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | |||||||
| chr4:38980185 | T | TAA | 52 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.823+6149_823+6150d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | |||||||
| chr4:38980185 | TA | T | 30 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(27): Show |
31 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.823+6150delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | |||||||
| chr4:38980205 | A | G | 1 | a0001c0001t0008g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.823+6131T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980205 | |||||||
| chr4:38980272 | T | C | 1 | a0001c0001t0009g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+6064A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980272 | |||||||
| chr4:38981033 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.823+5303C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981033 | |||||||
| chr4:38981131 | T | C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(42): Show |
45 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.823+5205A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981131 | |||||||
| chr4:38981135 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.823+5201G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981135 | |||||||
| chr4:38981174 | T | C | 3 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0015g0300 |
3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.823+5162A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981174 | |||||||
| chr4:38981223 | G | C | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+5113C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981223 | |||||||
| chr4:38981225 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823+5111C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981225 | |||||||
| chr4:38981240 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+5096G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981240 | |||||||
| chr4:38981348 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+4988T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981348 | |||||||
| chr4:38981363 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.823+4973C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981363 | |||||||
| chr4:38981410 | A | G | 1 | a0002c0002t0002g0357 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.823+4926T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981410 | |||||||
| chr4:38981436 | T | G | 1 | a0002c0002t0003g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.823+4900A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981436 | |||||||
| chr4:38981470 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.823+4866T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981470 | |||||||
| chr4:38981493 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+4843T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981493 | |||||||
| chr4:38981524 | G | A | 33 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(30): Show |
33 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+4812C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981524 | |||||||
| chr4:38981672 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+4664T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981672 | |||||||
| chr4:38981943 | G | A | 10 | a0001c0001t0001g0058 a0001c0001t0001g0196 a0001c0001t0001g0245 others(7): Show |
10 | HG01255.hp2 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+4393C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981943 | |||||||
| chr4:38981993 | A | G | 5 | a0002c0002t0001g0212 a0002c0002t0001g0286 a0002c0002t0002g0213 others(2): Show |
5 | HG00733.hp2 HG02083.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+4343T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981993 | |||||||
| chr4:38982016 | G | A | 7 | a0002c0002t0001g0253 a0004c0005t0001g0133 a0004c0005t0001g0200 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+4320C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982016 | |||||||
| chr4:38982092 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0131 others(52): Show |
56 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.823+4244G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982092 | |||||||
| chr4:38982140 | C | A | 3 | a0001c0001t0001g0046 a0001c0001t0002g0072 a0001c0001t0002g0079 |
3 | NA18969.hp2 NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.823+4196G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982140 | |||||||
| chr4:38982140 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.823+4196G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982140 | |||||||
| chr4:38982189 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(39): Show |
42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.823+4147G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982189 | |||||||
| chr4:38982223 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.823+4113C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982223 | |||||||
| chr4:38982305 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+4031A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982305 | |||||||
| chr4:38982385 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+3951G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982385 | |||||||
| chr4:38982899 | A | G | 1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823+3437T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982899 | |||||||
| chr4:38983077 | C | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+3259G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983077 | |||||||
| chr4:38983094 | G | C | 1 | a0002c0002t0001g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823+3242C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983094 | |||||||
| chr4:38983126 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.823+3210G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983126 | |||||||
| chr4:38983170 | C | G | 1 | a0001c0001t0002g0115 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.823+3166G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983170 | |||||||
| chr4:38983205 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.823+3131A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983205 | |||||||
| chr4:38983232 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.823+3104C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983232 | |||||||
| chr4:38983451 | T | C | 5 | a0001c0001t0001g0054 a0005c0006t0001g0029 a0005c0006t0001g0055 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2885A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983451 | |||||||
| chr4:38983514 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+2822A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983514 | |||||||
| chr4:38983748 | A | T | 3 | a0001c0001t0001g0255 a0001c0001t0005g0165 a0001c0001t0009g0376 |
3 | HG03453.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823+2588T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983748 | |||||||
| chr4:38983855 | C | T | 46 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(43): Show |
46 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+2481G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983855 | |||||||
| chr4:38984082 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(130): Show |
134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.823+2254C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984082 | |||||||
| chr4:38984185 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.823+2151G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984185 | |||||||
| chr4:38984199 | G | A | 2 | a0002c0002t0003g0221 a0002c0002t0003g0365 |
2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.823+2137C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984199 | |||||||
| chr4:38984325 | T | TTC | 6 | a0002c0002t0001g0253 a0004c0005t0001g0200 a0004c0005t0002g0254 others(3): Show |
6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2009_823+2010d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984325 | |||||||
| chr4:38984331 | CTG | C | 20 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(17): Show |
20 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+2003_823+2004d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984331 | |||||||
| chr4:38984333 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0091 others(58): Show |
62 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.823+2003C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984333 | |||||||
| chr4:38984333 | G | GTC | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0002c0002t0001g0298 |
3 | HG02451.hp2 HG03471.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.823+2001_823+2002d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984333 | |||||||
| chr4:38984335 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0091 others(57): Show |
61 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.823+2001G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984335 | |||||||
| chr4:38984337 | C | G | 20 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(17): Show |
20 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+1999G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984337 | |||||||
| chr4:38984345 | C | CTGTGTGT others(1): Show |
12 | a0001c0001t0001g0147 a0001c0001t0001g0181 a0001c0001t0001g0182 others(9): Show |
13 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+1990_823+1991i others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | |||||||
| chr4:38984345 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.823+1990_823+1991i others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | |||||||
| chr4:38984345 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0059 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+1990_823+1991i others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | |||||||
| chr4:38984345 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0005g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1990_823+1991i others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | |||||||
| chr4:38984347 | C | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(15): Show |
19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.823+1989G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | |||||||
| chr4:38984347 | CTCTGTG | C | 40 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(37): Show |
40 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.823+1983_823+1988d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | |||||||
| chr4:38984347 | CTCTGTGT others(3): Show |
C | 1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823+1979_823+1988d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | |||||||
| chr4:38984349 | C | CTG | 22 | a0001c0001t0001g0121 a0001c0001t0001g0139 a0001c0003t0001g0285 others(19): Show |
23 | HG00621.hp2 HG01934.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+1985_823+1986d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | C | CTGTG | 3 | a0002c0002t0002g0232 a0003c0004t0001g0204 a0003c0004t0001g0205 |
3 | HG02523.hp2 NA18944.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.823+1983_823+1986d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | C | G | 23 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(20): Show |
24 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.823+1987G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | CTG | C | 9 | a0001c0001t0002g0022 a0001c0001t0004g0240 a0001c0001t0005g0269 others(6): Show |
9 | HG00609.hp2 HG01175.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1985_823+1986d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | CTGTG | C | 89 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0090 others(86): Show |
89 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.823+1983_823+1986d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | CTGTGTG | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+1981_823+1986d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0255 a0001c0001t0001g0299 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+1979_823+1986d others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984349 | CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0004g0159 a0001c0001t0004g0170 a0001c0001t0004g0195 others(1): Show |
4 | HG01109.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1977_823+1986d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | |||||||
| chr4:38984351 | G | C | 54 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(51): Show |
54 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.823+1985C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984351 | |||||||
| chr4:38984353 | G | C | 48 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(45): Show |
48 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.823+1983C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984353 | |||||||
| chr4:38984355 | G | C | 42 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(39): Show |
42 | HG00423.hp1 HG01167.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.823+1981C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984355 | |||||||
| chr4:38984357 | G | C | 3 | a0001c0001t0001g0231 a0001c0001t0003g0093 a0001c0001t0003g0377 |
3 | HG02293.hp1 HG03942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.823+1979C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984357 | |||||||
| chr4:38984359 | G | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0255 a0001c0001t0001g0299 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1977C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984359 | |||||||
| chr4:38984361 | G | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0017 others(6): Show |
10 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+1975C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984361 | |||||||
| chr4:38984377 | GTGTGTGT | G | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+1952_823+1958d others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984377 | |||||||
| chr4:38984477 | G | GAC | 71 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(68): Show |
71 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+1857_823+1858d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984477 | |||||||
| chr4:38984563 | C | T | 5 | a0002c0002t0001g0038 a0002c0002t0001g0228 a0002c0002t0004g0050 others(2): Show |
5 | HG03669.hp2 HG03688.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1773G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984563 | |||||||
| chr4:38984614 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0017 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1722T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984614 | |||||||
| chr4:38984618 | T | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.823+1718A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984618 | |||||||
| chr4:38984685 | A | G | 6 | a0002c0002t0001g0253 a0004c0005t0001g0200 a0004c0005t0002g0254 others(3): Show |
6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+1651T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984685 | |||||||
| chr4:38984811 | C | T | 2 | a0002c0002t0001g0045 a0002c0002t0002g0356 |
2 | NA19000.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.823+1525G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984811 | |||||||
| chr4:38984997 | C | CA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0058 others(155): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+1338_823+1339i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984997 | |||||||
| chr4:38985152 | G | T | 115 | a0001c0001t0001g0023 a0001c0001t0001g0121 a0001c0001t0001g0139 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.823+1184C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985152 | |||||||
| chr4:38985159 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0004g0009 a0001c0001t0004g0304 others(3): Show |
6 | HG02015.hp2 HG02080.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+1177C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985159 | |||||||
| chr4:38985211 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823+1125G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985211 | |||||||
| chr4:38985443 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0131 others(28): Show |
32 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.823+893G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985443 | |||||||
| chr4:38985475 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.823+861C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985475 | |||||||
| chr4:38985554 | C | T | 4 | a0002c0002t0001g0038 a0002c0002t0001g0228 a0002c0002t0004g0050 others(1): Show |
4 | HG03688.hp1 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+782G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985554 | |||||||
| chr4:38985616 | A | G | 15 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(12): Show |
16 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+720T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985616 | |||||||
| chr4:38985647 | C | T | 1 | a0002c0002t0002g0225 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.823+689G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985647 | |||||||
| chr4:38985702 | T | C | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+634A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985702 | |||||||
| chr4:38985795 | G | C | 1 | a0001c0001t0005g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.823+541C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985795 | |||||||
| chr4:38985812 | A | C | 3 | a0001c0001t0001g0257 a0001c0001t0002g0044 a0001c0001t0005g0040 |
3 | HG02717.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.823+524T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985812 | |||||||
| chr4:38985863 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0002g0296 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.823+473A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985863 | |||||||
| chr4:38985927 | T | C | 1 | a0001c0001t0005g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+409A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985927 | |||||||
| chr4:38986083 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+253G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986083 | |||||||
| chr4:38986089 | A | G | 11 | a0001c0001t0001g0263 a0001c0001t0002g0028 a0001c0001t0002g0268 others(8): Show |
11 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+247T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986089 | |||||||
| chr4:38986090 | C | T | 48 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0059 others(45): Show |
49 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.823+246G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986090 | |||||||
| chr4:38986205 | A | G | 3 | a0002c0002t0001g0082 a0002c0002t0001g0084 a0002c0002t0001g0111 |
3 | HG00140.hp2 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.823+131T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986205 | |||||||
| chr4:38986462 | C | T | 29 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(26): Show |
29 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.740-43G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986462 | |||||||
| chr4:38986512 | A | G | 9 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(6): Show |
9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-93T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986512 | |||||||
| chr4:38986604 | C | G | 2 | a0001c0001t0001g0255 a0001c0001t0005g0165 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-185G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986604 | |||||||
| chr4:38986618 | C | T | 1 | a0001c0001t0004g0329 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.740-199G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986618 | |||||||
| chr4:38986679 | A | G | 3 | a0001c0001t0002g0163 a0001c0001t0009g0302 a0001c0001t0009g0376 |
3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-260T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986679 | |||||||
| chr4:38986729 | A | G | 3 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0015g0300 |
3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.740-310T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986729 | |||||||
| chr4:38986780 | C | A | 9 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(6): Show |
9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-361G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986780 | |||||||
| chr4:38986786 | C | T | 40 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(37): Show |
40 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.740-367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986786 | |||||||
| chr4:38986787 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.740-368C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986787 | |||||||
| chr4:38986807 | CAA | C | 14 | a0001c0001t0001g0047 a0001c0001t0001g0090 a0001c0001t0001g0131 others(11): Show |
14 | HG01952.hp2 HG01981.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-390_740-389del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAA | C | 43 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(40): Show |
43 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.740-391_740-389del others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAA | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0188 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.740-393_740-389del others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAA | C | 25 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0162 others(22): Show |
25 | HG01070.hp1 HG01256.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.740-394_740-389del others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0109 others(20): Show |
24 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.740-395_740-389del others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0005g0165 a0001c0001t0005g0264 a0001c0001t0005g0269 others(12): Show |
15 | HG00741.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-396_740-389del others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(2): Show |
C | 37 | a0001c0001t0001g0023 a0002c0002t0001g0027 a0002c0002t0001g0031 others(34): Show |
38 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.740-397_740-389del others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(3): Show |
C | 50 | a0001c0001t0001g0121 a0001c0001t0001g0139 a0001c0001t0002g0326 others(47): Show |
51 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.740-398_740-389del others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(4): Show |
C | 8 | a0002c0002t0001g0252 a0002c0002t0001g0253 a0002c0002t0001g0262 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.740-399_740-389del others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(5): Show |
C | 2 | a0006c0007t0003g0288 a0006c0007t0006g0289 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.740-400_740-389del others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0163 a0001c0001t0009g0302 a0001c0001t0009g0376 |
3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-401_740-389del others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0017 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-403_740-389del others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0299 a0001c0001t0002g0203 a0001c0001t0015g0300 |
3 | HG02922.hp2 HG02965.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.740-404_740-389del others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.740-405_740-389del others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(12): Show |
C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0078 others(6): Show |
9 | HG00099.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-407_740-389del others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(13): Show |
C | 4 | a0001c0001t0001g0114 a0001c0001t0002g0115 a0001c0001t0012g0098 others(1): Show |
4 | HG02015.hp2 NA18612.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-408_740-389del others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(14): Show |
C | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG01993.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-409_740-389del others(21): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(15): Show |
C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0124 a0001c0001t0004g0103 |
3 | HG00609.hp1 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.740-410_740-389del others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.740-411_740-389del others(23): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.740-413_740-389del others(25): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(19): Show |
C | 1 | a0002c0002t0002g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.740-414_740-389del others(26): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.740-415_740-389del others(27): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(22): Show |
C | 2 | a0002c0002t0001g0212 a0002c0002t0004g0138 |
2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.740-417_740-389del others(29): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986807 | CAAAAAAA others(25): Show |
C | 1 | a0001c0001t0001g0343 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740-420_740-389del others(32): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | |||||||
| chr4:38986829 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0017 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-410T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986829 | |||||||
| chr4:38986882 | T | C | 2 | a0001c0003t0002g0187 a0001c0003t0002g0190 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.740-463A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986882 | |||||||
| chr4:38986896 | A | C | 2 | a0001c0001t0001g0255 a0001c0001t0005g0165 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-477T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986896 | |||||||
| chr4:38986900 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0009g0302 a0001c0001t0009g0376 |
3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-481A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986900 | |||||||
| chr4:38986912 | T | C | 1 | a0004c0005t0002g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.740-493A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986912 | |||||||
| chr4:38986967 | G | A | 113 | a0001c0001t0001g0023 a0001c0001t0001g0121 a0001c0001t0001g0139 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.740-548C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986967 | |||||||
| chr4:38986976 | CA | C | 18 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(15): Show |
19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.740-558delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986976 | |||||||
| chr4:38987001 | G | T | 40 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(37): Show |
40 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.740-582C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987001 | |||||||
| chr4:38987086 | C | T | 1 | a0001c0001t0002g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.740-667G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987086 | |||||||
| chr4:38987196 | T | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(40): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.740-777A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987196 | |||||||
| chr4:38987499 | A | G | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.740-1080T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987499 | |||||||
| chr4:38987689 | T | C | 31 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(28): Show |
31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.739+1162A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987689 | |||||||
| chr4:38987845 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+1006T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987845 | |||||||
| chr4:38987928 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0247 a0001c0001t0001g0354 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.739+923A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987928 | |||||||
| chr4:38987940 | T | C | 3 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0015g0300 |
3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.739+911A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987940 | |||||||
| chr4:38988063 | C | T | 1 | a0002c0002t0003g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.739+788G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988063 | |||||||
| chr4:38988127 | G | A | 23 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(20): Show |
23 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+724C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988127 | |||||||
| chr4:38988172 | C | T | 33 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(30): Show |
33 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.739+679G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988172 | |||||||
| chr4:38988178 | T | C | 2 | a0002c0002t0001g0284 a0002c0002t0003g0280 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.739+673A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988178 | |||||||
| chr4:38988187 | C | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0131 others(28): Show |
32 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.739+664G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988187 | |||||||
| chr4:38988320 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.739+531G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988320 | |||||||
| chr4:38988372 | C | T | 9 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(6): Show |
9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+479G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988372 | |||||||
| chr4:38988416 | C | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(203): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.739+435G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988416 | |||||||
| chr4:38988434 | GGCTGGTC others(1): Show |
G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.739+409_739+416del others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988434 | |||||||
| chr4:38988474 | C | A | 19 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(16): Show |
20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.739+377G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988474 | |||||||
| chr4:38988509 | G | A | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739+342C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988509 | |||||||
| chr4:38988512 | ATGAGTCA others(12): Show |
A | 1 | a0001c0001t0004g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.739+320_739+338del others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988512 | |||||||
| chr4:38988526 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(203): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.739+325A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988526 | |||||||
| chr4:38988610 | T | C | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.739+241A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988610 | |||||||
| chr4:38988645 | T | C | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.739+206A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988645 | |||||||
| chr4:38988651 | T | TACTC | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.739+199_739+200ins others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988651 | |||||||
| chr4:38988684 | T | C | 3 | a0004c0005t0001g0200 a0004c0005t0003g0201 a0004c0005t0005g0249 |
3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.739+167A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988684 | |||||||
| chr4:38988714 | C | T | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.739+137G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988714 | |||||||
| chr4:38988716 | T | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.739+135A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988716 | |||||||
| chr4:38988763 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+88C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988763 | |||||||
| chr4:38988808 | G | C | 1 | a0002c0002t0001g0324 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.739+43C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988808 | |||||||
| chr4:38988824 | C | T | 1 | a0001c0001t0004g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.739+27G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988824 | |||||||
| chr4:38989030 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0003g0153 |
2 | NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.620-60A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989030 | |||||||
| chr4:38989159 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0002g0316 |
2 | NA18964.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.620-189G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989159 | |||||||
| chr4:38989164 | A | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(15): Show |
19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.620-194T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989164 | |||||||
| chr4:38989507 | G | A | 3 | a0004c0005t0001g0200 a0004c0005t0003g0201 a0004c0005t0005g0249 |
3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.620-537C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989507 | |||||||
| chr4:38989621 | A | G | 19 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(16): Show |
20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.620-651T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989621 | |||||||
| chr4:38989635 | T | G | 278 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.620-665A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989635 | |||||||
| chr4:38989638 | A | G | 28 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(25): Show |
28 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.620-668T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989638 | |||||||
| chr4:38989641 | A | T | 27 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(24): Show |
27 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.620-671T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989641 | |||||||
| chr4:38989669 | A | G | 27 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(24): Show |
27 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.620-699T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989669 | |||||||
| chr4:38989752 | C | G | 1 | a0001c0001t0002g0301 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.620-782G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989752 | |||||||
| chr4:38989768 | TTTTTA | T | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.620-803_620-799del others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989768 | |||||||
| chr4:38989770 | T | TTTATTTT others(13): Show |
1 | a0001c0001t0003g0297 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.620-820_620-801dup others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989770 | |||||||
| chr4:38989770 | TTTATTTT others(13): Show |
T | 1 | a0001c0001t0009g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.620-820_620-801del others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989770 | |||||||
| chr4:38989790 | C | CTTATT | 3 | a0001c0001t0001g0255 a0001c0001t0005g0165 a0002c0002t0001g0363 |
3 | HG01361.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.620-825_620-821dup others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989790 | |||||||
| chr4:38989889 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.620-919A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989889 | |||||||
| chr4:38989892 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.620-922G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989892 | |||||||
| chr4:38989956 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0002g0068 a0001c0001t0004g0240 |
3 | HG01175.hp2 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.620-986C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989956 | |||||||
| chr4:38989987 | G | T | 1 | a0001c0001t0003g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620-1017C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989987 | |||||||
| chr4:38990042 | G | A | 1 | a0002c0002t0002g0213 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.620-1072C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990042 | |||||||
| chr4:38990087 | A | G | 1 | a0001c0001t0005g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.620-1117T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990087 | |||||||
| chr4:38990148 | G | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(228): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.620-1178C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990148 | |||||||
| chr4:38990238 | C | A | 31 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(28): Show |
31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.620-1268G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990238 | |||||||
| chr4:38990294 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.620-1324C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990294 | |||||||
| chr4:38990337 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.620-1367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990337 | |||||||
| chr4:38990357 | A | G | 2 | a0001c0001t0002g0261 a0001c0009t0001g0176 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.620-1387T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990357 | |||||||
| chr4:38990390 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0130 |
2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.620-1420G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990390 | |||||||
| chr4:38990394 | C | T | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.620-1424G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990394 | |||||||
| chr4:38990530 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.620-1560T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990530 | |||||||
| chr4:38990531 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(224): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.620-1561T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990531 | |||||||
| chr4:38990556 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0041 others(147): Show |
153 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.620-1586T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990556 | |||||||
| chr4:38990612 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.620-1642A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990612 | |||||||
| chr4:38990626 | C | A | 59 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-1656G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990626 | |||||||
| chr4:38990628 | C | T | 1 | a0001c0003t0002g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.620-1658G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990628 | |||||||
| chr4:38990659 | A | G | 236 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.620-1689T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990659 | |||||||
| chr4:38990679 | A | C | 1 | a0001c0003t0004g0334 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.620-1709T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990679 | |||||||
| chr4:38990685 | G | A | 236 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.620-1715C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990685 | |||||||
| chr4:38990745 | G | C | 237 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(234): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.620-1775C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990745 | |||||||
| chr4:38990750 | C | G | 237 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(234): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.620-1780G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990750 | |||||||
| chr4:38990774 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.620-1804G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990774 | |||||||
| chr4:38990791 | G | T | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.620-1821C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990791 | |||||||
| chr4:38990820 | T | A | 1 | a0001c0003t0004g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.620-1850A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990820 | |||||||
| chr4:38990830 | G | GT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0140 others(20): Show |
23 | HG01175.hp1 HG01978.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.620-1861dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTC | 33 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(30): Show |
33 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.620-1861_620-1860i others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTT | 17 | a0001c0001t0001g0058 a0001c0001t0001g0131 a0001c0001t0001g0164 others(14): Show |
17 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.620-1864_620-1861d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTT | 12 | a0001c0001t0001g0169 a0001c0001t0001g0196 a0001c0001t0001g0272 others(9): Show |
12 | HG01243.hp1 HG01433.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1865_620-1861d others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0037 a0001c0001t0001g0332 a0001c0001t0001g0341 others(3): Show |
6 | HG02129.hp1 HG02165.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.620-1873_620-1861d others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0078 a0001c0001t0001g0275 a0001c0001t0003g0337 others(1): Show |
4 | HG00438.hp1 HG02145.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1874_620-1861d others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0336 a0001c0001t0002g0108 a0001c0001t0011g0069 |
3 | NA19001.hp2 NA19074.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.620-1875_620-1861d others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0117 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.620-1861_620-1860i others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0368 others(1): Show |
4 | HG00544.hp1 NA18968.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-1876_620-1861d others(18): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(10): Show |
7 | a0001c0001t0001g0034 a0001c0001t0001g0086 a0001c0001t0001g0279 others(4): Show |
7 | HG00609.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-1877_620-1861d others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(11): Show |
5 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0047 others(2): Show |
5 | HG01074.hp1 HG01361.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.620-1878_620-1861d others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(12): Show |
9 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0002g0072 others(6): Show |
9 | HG00099.hp2 HG01952.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.620-1879_620-1861d others(21): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | G | GTTTTTTT others(14): Show |
1 | a0001c0001t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.620-1881_620-1861d others(23): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990830 | GT | G | 7 | a0001c0001t0001g0303 a0001c0001t0002g0292 a0001c0001t0005g0269 others(4): Show |
7 | HG00597.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-1861delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | |||||||
| chr4:38990831 | T | TTTC | 107 | a0001c0001t0001g0023 a0001c0001t0003g0070 a0001c0001t0003g0153 others(104): Show |
109 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.620-1862_620-1861i others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990831 | |||||||
| chr4:38990835 | T | TTTTTTTT others(11): Show |
17 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(14): Show |
18 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.620-1866_620-1865i others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990835 | |||||||
| chr4:38990841 | T | TTGTTTTG others(11): Show |
1 | a0001c0001t0005g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.620-1872_620-1871i others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990841 | |||||||
| chr4:38990886 | T | A | 2 | a0001c0001t0002g0028 a0001c0001t0005g0290 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.620-1916A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990886 | |||||||
| chr4:38990889 | G | A | 208 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.620-1919C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990889 | |||||||
| chr4:38990902 | C | T | 208 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.620-1932G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990902 | |||||||
| chr4:38990909 | C | G | 4 | a0001c0001t0003g0265 a0001c0001t0005g0251 a0001c0001t0005g0264 others(1): Show |
4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1939G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990909 | |||||||
| chr4:38990927 | G | A | 208 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.620-1957C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990927 | |||||||
| chr4:38990929 | G | A | 6 | a0001c0001t0002g0171 a0001c0001t0002g0199 a0001c0001t0002g0260 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1959C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990929 | |||||||
| chr4:38990939 | G | T | 209 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.620-1969C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990939 | |||||||
| chr4:38990959 | G | A | 209 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.620-1989C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990959 | |||||||
| chr4:38991084 | C | G | 3 | a0001c0001t0001g0257 a0001c0001t0002g0044 a0001c0001t0005g0040 |
3 | HG02717.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.620-2114G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991084 | |||||||
| chr4:38991133 | T | C | 199 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.620-2163A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991133 | |||||||
| chr4:38991206 | C | CT | 177 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(174): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.620-2237dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991206 | |||||||
| chr4:38991206 | C | CTT | 19 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(16): Show |
20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.620-2238_620-2237d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991206 | |||||||
| chr4:38991212 | C | T | 199 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.620-2242G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991212 | |||||||
| chr4:38991227 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.620-2258dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991227 | |||||||
| chr4:38991227 | CT | C | 8 | a0002c0002t0002g0141 a0003c0004t0003g0012 a0004c0005t0001g0200 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.620-2258delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991227 | |||||||
| chr4:38991381 | T | C | 200 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.619+2357A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991381 | |||||||
| chr4:38991477 | T | C | 1 | a0001c0001t0001g0345 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.619+2261A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991477 | |||||||
| chr4:38991540 | C | T | 2 | a0002c0002t0001g0236 a0002c0002t0002g0233 |
2 | HG02738.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.619+2198G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991540 | |||||||
| chr4:38991564 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(39): Show |
42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.619+2174G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991564 | |||||||
| chr4:38991574 | A | G | 158 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(155): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.619+2164T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991574 | |||||||
| chr4:38991674 | AAC | A | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+2062_619+2063d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991674 | |||||||
| chr4:38991758 | G | A | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+1980C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991758 | |||||||
| chr4:38991803 | A | G | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+1935T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991803 | |||||||
| chr4:38991890 | T | C | 1 | a0002c0002t0004g0227 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.619+1848A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991890 | |||||||
| chr4:38991899 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.619+1839T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991899 | |||||||
| chr4:38991951 | C | A | 14 | a0002c0002t0001g0019 a0002c0002t0001g0064 a0002c0002t0002g0003 others(11): Show |
15 | HG02071.hp2 NA18747.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.619+1787G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991951 | |||||||
| chr4:38992003 | G | A | 153 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.619+1735C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992003 | |||||||
| chr4:38992005 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.619+1733C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992005 | |||||||
| chr4:38992032 | C | A | 1 | a0002c0002t0002g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.619+1706G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992032 | |||||||
| chr4:38992064 | G | A | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+1674C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992064 | |||||||
| chr4:38992168 | G | A | 3 | a0002c0002t0001g0191 a0002c0002t0003g0052 a0002c0002t0003g0085 |
3 | HG02300.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.619+1570C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992168 | |||||||
| chr4:38992409 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.619+1329C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992409 | |||||||
| chr4:38992475 | A | C | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+1263T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992475 | |||||||
| chr4:38992535 | T | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.619+1203A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992535 | |||||||
| chr4:38992567 | G | T | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.619+1171C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992567 | |||||||
| chr4:38992611 | G | C | 1 | a0001c0001t0009g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.619+1127C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992611 | |||||||
| chr4:38992665 | CATATATA others(54): Show |
C | 2 | a0001c0001t0005g0168 a0001c0001t0010g0167 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+1012_619+1072d others(63): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992665 | |||||||
| chr4:38992667 | TATATATA others(61): Show |
T | 153 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.619+1003_619+1070d others(70): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992667 | |||||||
| chr4:38992679 | ATATTATA others(62): Show |
A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(18): Show |
22 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.619+990_619+1058de others(70): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992679 | |||||||
| chr4:38992681 | AT | A | 31 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(28): Show |
31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.619+1056delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992681 | |||||||
| chr4:38992681 | ATTATATA others(75): Show |
A | 4 | a0001c0001t0003g0265 a0001c0001t0005g0251 a0001c0001t0005g0264 others(1): Show |
4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.619+975_619+1056de others(83): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992681 | |||||||
| chr4:38992682 | T | TATATAA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+1055_619+1056i others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | |||||||
| chr4:38992682 | T | TTATATAA others(40): Show |
1 | a0001c0001t0001g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.619+1009_619+1055d others(49): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | |||||||
| chr4:38992682 | T | TTATATAA others(47): Show |
1 | a0001c0003t0004g0334 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.619+1002_619+1055d others(56): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | |||||||
| chr4:38992686 | A | ATTAT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+1051_619+1052i others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992686 | |||||||
| chr4:38992686 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.619+1052T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992686 | |||||||
| chr4:38992700 | AAT | A | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.619+1036_619+1037d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992700 | |||||||
| chr4:38992701 | A | ATATATAT others(2): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0091 others(21): Show |
25 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.619+1028_619+1036d others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992701 | |||||||
| chr4:38992702 | T | TATATATA others(13): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0017 |
3 | HG02145.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.619+1035_619+1036i others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | |||||||
| chr4:38992702 | T | TATATATA others(24): Show |
2 | a0001c0001t0001g0255 a0001c0001t0005g0165 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.619+1035_619+1036i others(33): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | |||||||
| chr4:38992702 | T | TATATATA others(79): Show |
1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.619+1035_619+1036i others(88): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | |||||||
| chr4:38992703 | A | ATATATAT others(4): Show |
2 | a0004c0005t0001g0200 a0004c0005t0003g0201 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.619+1034_619+1035i others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992703 | |||||||
| chr4:38992703 | A | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.619+1035T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992703 | |||||||
| chr4:38992706 | T | TATATATT others(29): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0366 |
2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.619+996_619+1031du others(37): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992706 | |||||||
| chr4:38992713 | T | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(29): Show |
33 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.619+1025A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992713 | |||||||
| chr4:38992714 | A | T | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.619+1024T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992714 | |||||||
| chr4:38992715 | T | A | 2 | a0001c0001t0002g0292 a0001c0001t0003g0106 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.619+1023A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992715 | |||||||
| chr4:38992724 | A | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0140 a0001c0001t0001g0149 others(1): Show |
4 | HG00639.hp2 HG01175.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.619+1014T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992724 | |||||||
| chr4:38992747 | AT | A | 112 | a0001c0001t0001g0023 a0001c0001t0005g0168 a0001c0001t0010g0167 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.619+990delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992747 | |||||||
| chr4:38992748 | T | TA | 43 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(40): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.619+989_619+990ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992748 | |||||||
| chr4:38992748 | TTA | T | 3 | a0004c0005t0001g0200 a0004c0005t0003g0201 a0004c0005t0005g0249 |
3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.619+988_619+989del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992748 | |||||||
| chr4:38992758 | A | T | 1 | a0001c0001t0003g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.619+980T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992758 | |||||||
| chr4:38992760 | A | T | 16 | a0001c0001t0001g0131 a0001c0001t0001g0164 a0001c0001t0001g0169 others(13): Show |
16 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.619+978T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992760 | |||||||
| chr4:38992762 | A | T | 46 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0117 others(43): Show |
46 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.619+976T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992762 | |||||||
| chr4:38992762 | AT | A | 22 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(19): Show |
22 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.619+975delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992762 | |||||||
| chr4:38992764 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.619+974A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992764 | |||||||
| chr4:38992766 | T | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0299 others(7): Show |
11 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.619+972A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992766 | |||||||
| chr4:38992772 | G | T | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+966C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992772 | |||||||
| chr4:38992831 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619+907C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992831 | |||||||
| chr4:38992847 | C | T | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+891G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992847 | |||||||
| chr4:38992892 | C | G | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+846G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992892 | |||||||
| chr4:38992912 | C | A | 1 | a0002c0002t0003g0085 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619+826G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992912 | |||||||
| chr4:38992921 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0008g0063 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.619+817G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992921 | |||||||
| chr4:38992929 | T | A | 42 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(39): Show |
42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.619+809A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992929 | |||||||
| chr4:38992951 | C | T | 1 | a0001c0003t0003g0351 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.619+787G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992951 | |||||||
| chr4:38993013 | A | G | 177 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.619+725T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993013 | |||||||
| chr4:38993050 | C | T | 2 | a0001c0001t0005g0168 a0001c0001t0010g0167 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+688G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993050 | |||||||
| chr4:38993146 | A | G | 2 | a0001c0001t0005g0168 a0001c0001t0010g0167 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+592T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993146 | |||||||
| chr4:38993255 | C | A | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+483G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993255 | |||||||
| chr4:38993258 | C | T | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+480G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993258 | |||||||
| chr4:38993261 | C | T | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.619+477G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993261 | |||||||
| chr4:38993344 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.619+394A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993344 | |||||||
| chr4:38993399 | T | C | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.619+339A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993399 | |||||||
| chr4:38993461 | TA | T | 155 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.619+276delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993461 | |||||||
| chr4:38993690 | A | G | 157 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(154): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.619+48T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993690 | |||||||
| chr4:38993698 | C | T | 8 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.619+40G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993698 | |||||||
| chr4:38994108 | G | A | 5 | a0001c0003t0001g0186 a0001c0003t0002g0187 a0001c0003t0002g0190 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-110C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994108 | |||||||
| chr4:38994291 | A | G | 159 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(156): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.359-293T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994291 | |||||||
| chr4:38994363 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.359-365C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994363 | |||||||
| chr4:38994441 | A | G | 114 | a0001c0001t0001g0023 a0002c0002t0001g0019 a0002c0002t0001g0027 others(111): Show |
116 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.359-443T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994441 | |||||||
| chr4:38994509 | A | C | 185 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.359-511T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994509 | |||||||
| chr4:38994567 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-569T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994567 | |||||||
| chr4:38994614 | G | A | 163 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-616C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994614 | |||||||
| chr4:38994672 | A | G | 185 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.359-674T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994672 | |||||||
| chr4:38994679 | C | T | 163 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-681G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994679 | |||||||
| chr4:38994684 | C | T | 163 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-686G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994684 | |||||||
| chr4:38994721 | G | A | 20 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(17): Show |
21 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-723C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994721 | |||||||
| chr4:38994764 | A | G | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.359-766T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994764 | |||||||
| chr4:38994808 | C | T | 1 | a0001c0001t0005g0060 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.359-810G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994808 | |||||||
| chr4:38994821 | G | A | 20 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(17): Show |
21 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-823C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994821 | |||||||
| chr4:38994852 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-854G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994852 | |||||||
| chr4:38994873 | C | G | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.359-875G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994873 | |||||||
| chr4:38994952 | A | C | 3 | a0004c0005t0002g0254 a0004c0005t0002g0258 a0004c0005t0005g0249 |
3 | HG02622.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.359-954T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994952 | |||||||
| chr4:38995054 | G | A | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.359-1056C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995054 | |||||||
| chr4:38995142 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0366 a0001c0001t0002g0296 |
3 | HG01255.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.359-1144C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995142 | |||||||
| chr4:38995159 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.359-1161G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995159 | |||||||
| chr4:38995222 | A | G | 163 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-1224T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995222 | |||||||
| chr4:38995246 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-1248C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995246 | |||||||
| chr4:38995282 | G | T | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-1284C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995282 | |||||||
| chr4:38995408 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.359-1410G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995408 | |||||||
| chr4:38995534 | A | G | 162 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.359-1536T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995534 | |||||||
| chr4:38995604 | A | C | 162 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.359-1606T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995604 | |||||||
| chr4:38995609 | G | A | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.359-1611C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995609 | |||||||
| chr4:38995656 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-1658T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995656 | |||||||
| chr4:38995677 | T | C | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.359-1679A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995677 | |||||||
| chr4:38995688 | C | T | 1 | a0001c0001t0003g0325 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.359-1690G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995688 | |||||||
| chr4:38995850 | G | T | 3 | a0004c0005t0001g0200 a0004c0005t0003g0201 a0004c0005t0005g0249 |
3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.359-1852C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995850 | |||||||
| chr4:38995852 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.359-1854A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995852 | |||||||
| chr4:38995873 | A | T | 1 | a0001c0003t0003g0351 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.359-1875T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995873 | |||||||
| chr4:38995971 | T | A | 69 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.359-1973A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995971 | |||||||
| chr4:38996237 | C | T | 1 | a0002c0002t0002g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.359-2239G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996237 | |||||||
| chr4:38996262 | G | GA | 69 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.359-2265dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996262 | |||||||
| chr4:38996262 | GA | G | 10 | a0001c0001t0001g0121 a0001c0001t0001g0255 a0001c0001t0002g0171 others(7): Show |
10 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-2265delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996262 | |||||||
| chr4:38996275 | AAG | A | 105 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(102): Show |
107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.359-2279_359-2278d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996275 | |||||||
| chr4:38996276 | A | AC | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-2279_359-2278i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996276 | |||||||
| chr4:38996276 | AG | A | 7 | a0002c0002t0001g0119 a0002c0002t0002g0129 a0002c0002t0003g0294 others(4): Show |
7 | HG02559.hp2 HG04184.hp2 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-2279delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996276 | |||||||
| chr4:38996324 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.358+2316G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996324 | |||||||
| chr4:38996389 | C | T | 113 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+2251G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996389 | |||||||
| chr4:38996406 | C | CA | 17 | a0001c0001t0002g0108 a0001c0001t0003g0024 a0002c0002t0001g0031 others(14): Show |
17 | HG01433.hp1 HG02135.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.358+2233dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | |||||||
| chr4:38996406 | C | CAA | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+2232_358+2233d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | |||||||
| chr4:38996406 | CA | C | 18 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0255 others(15): Show |
18 | HG01975.hp1 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.358+2233delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | |||||||
| chr4:38996497 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.358+2143T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996497 | |||||||
| chr4:38996597 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.358+2043G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996597 | |||||||
| chr4:38996604 | G | A | 113 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+2036C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996604 | |||||||
| chr4:38996672 | C | A | 5 | a0001c0001t0002g0171 a0001c0001t0002g0199 a0001c0001t0003g0173 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+1968G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996672 | |||||||
| chr4:38996829 | G | A | 45 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(42): Show |
45 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+1811C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996829 | |||||||
| chr4:38996972 | A | G | 1 | a0002c0002t0004g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.358+1668T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996972 | |||||||
| chr4:38997068 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358+1572T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997068 | |||||||
| chr4:38997077 | C | T | 1 | a0001c0001t0004g0103 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.358+1563G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997077 | |||||||
| chr4:38997086 | G | C | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+1554C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997086 | |||||||
| chr4:38997153 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+1487A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997153 | |||||||
| chr4:38997347 | C | T | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1293G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997347 | |||||||
| chr4:38997412 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.358+1228T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997412 | |||||||
| chr4:38997439 | TA | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0199 a0001c0001t0003g0173 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+1200delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997439 | |||||||
| chr4:38997542 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358+1098T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997542 | |||||||
| chr4:38997646 | G | T | 5 | a0001c0001t0001g0054 a0001c0003t0001g0353 a0001c0003t0001g0367 others(2): Show |
5 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+994C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997646 | |||||||
| chr4:38997828 | A | G | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+812T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997828 | |||||||
| chr4:38997937 | A | C | 1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.358+703T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997937 | |||||||
| chr4:38997958 | T | A | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+682A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997958 | |||||||
| chr4:38997968 | G | A | 69 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.358+672C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997968 | |||||||
| chr4:38998103 | A | G | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+537T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998103 | |||||||
| chr4:38998174 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(196): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.358+466C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998174 | |||||||
| chr4:38998267 | A | G | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+373T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998267 | |||||||
| chr4:38998271 | G | T | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+369C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998271 | |||||||
| chr4:38998310 | G | A | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+330C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998310 | |||||||
| chr4:38998352 | T | C | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+288A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998352 | |||||||
| chr4:38998412 | C | T | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+228G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998412 | |||||||
| chr4:38998523 | A | G | 118 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+117T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998523 | |||||||
| chr4:38998543 | C | CAAA | 113 | a0002c0002t0001g0019 a0002c0002t0001g0027 a0002c0002t0001g0031 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+94_358+96dupTT others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998543 | |||||||
| chr4:38998543 | CA | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
11 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+96delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998543 | |||||||
| chr4:38998571 | T | A | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+69A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998571 | |||||||
| chr4:38998936 | C | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0124 a0001c0001t0004g0103 |
3 | HG00609.hp1 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.89-27G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38998936 | |||||||
| chr4:38998949 | C | T | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-40G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38998949 | |||||||
| chr4:38999022 | G | T | 69 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.89-113C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999022 | |||||||
| chr4:38999029 | A | G | 123 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-120T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999029 | |||||||
| chr4:38999110 | AT | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0021 others(164): Show |
168 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.89-202delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | |||||||
| chr4:38999110 | ATT | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0375 a0001c0001t0002g0115 others(3): Show |
6 | HG00423.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-203_89-202delAA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | |||||||
| chr4:38999110 | ATTTTTT | A | 112 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.89-207_89-202delAA others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | |||||||
| chr4:38999110 | ATTTTTTT others(3): Show |
A | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-211_89-202delAA others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | |||||||
| chr4:38999111 | T | TTTA | 69 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0036 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.89-203_89-202insTA others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999111 | |||||||
| chr4:38999114 | T | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0341 a0001c0001t0002g0296 others(2): Show |
5 | HG01361.hp1 HG02165.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-205A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999114 | |||||||
| chr4:38999114 | T | TA | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-206_89-205insT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999114 | |||||||
| chr4:38999115 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0021 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.89-206A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999115 | |||||||
| chr4:38999116 | T | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0375 a0001c0001t0002g0115 others(3): Show |
6 | HG00280.hp2 HG00423.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-207A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999116 | |||||||
| chr4:38999118 | T | A | 13 | a0001c0001t0001g0018 a0001c0001t0001g0196 a0001c0001t0001g0245 others(10): Show |
13 | HG01255.hp2 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.89-209A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999118 | |||||||
| chr4:38999119 | T | A | 119 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(116): Show |
120 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-210A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999119 | |||||||
| chr4:38999120 | T | A | 145 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0036 others(142): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.89-211A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999120 | |||||||
| chr4:38999123 | T | A | 39 | a0001c0001t0001g0059 a0001c0001t0001g0121 a0001c0001t0001g0139 others(36): Show |
40 | HG00099.hp1 HG00544.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-214A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999123 | |||||||
| chr4:38999124 | T | A | 8 | a0002c0002t0001g0239 a0002c0002t0001g0243 a0002c0002t0001g0298 others(5): Show |
8 | HG00621.hp2 HG00673.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-215A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999124 | |||||||
| chr4:38999125 | T | A | 4 | a0001c0001t0003g0265 a0001c0001t0005g0251 a0001c0001t0005g0264 others(1): Show |
4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-216A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999125 | |||||||
| chr4:38999127 | T | A | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-218A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999127 | |||||||
| chr4:38999128 | T | A | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-219A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999128 | |||||||
| chr4:38999174 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-265A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999174 | |||||||
| chr4:38999180 | A | G | 1 | a0001c0001t0004g0081 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.89-271T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999180 | |||||||
| chr4:38999190 | T | C | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-281A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999190 | |||||||
| chr4:38999456 | CCTTAGAT others(1): Show |
C | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-555_89-548delAA others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999456 | |||||||
| chr4:38999698 | T | A | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-789A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999698 | |||||||
| chr4:38999987 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.89-1078G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999987 | |||||||
| chr4:38999990 | A | C | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1081T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999990 | |||||||
| chr4:39000047 | A | C | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1138T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000047 | |||||||
| chr4:39000094 | CA | C | 5 | a0002c0002t0001g0082 a0002c0002t0001g0111 a0002c0002t0002g0061 others(2): Show |
5 | HG00741.hp2 HG01192.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1186delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000094 | |||||||
| chr4:39000101 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89-1192G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000101 | |||||||
| chr4:39000105 | C | T | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1196G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000105 | |||||||
| chr4:39000120 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.89-1211C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000120 | |||||||
| chr4:39000137 | T | C | 2 | a0002c0002t0002g0011 a0002c0002t0002g0335 |
2 | HG00609.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.89-1228A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000137 | |||||||
| chr4:39000253 | G | A | 1 | a0001c0001t0006g0340 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.89-1344C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000253 | |||||||
| chr4:39000289 | T | G | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1380A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000289 | |||||||
| chr4:39000327 | A | G | 1 | a0001c0003t0006g0348 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.89-1418T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000327 | |||||||
| chr4:39000338 | A | G | 123 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1429T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000338 | |||||||
| chr4:39000379 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.89-1470C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000379 | |||||||
| chr4:39000468 | C | T | 8 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1559G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000468 | |||||||
| chr4:39000563 | T | C | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | NA19056.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.89-1654A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000563 | |||||||
| chr4:39000565 | G | A | 69 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.89-1656C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000565 | |||||||
| chr4:39000570 | T | C | 123 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1661A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000570 | |||||||
| chr4:39000613 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0004g0009 a0001c0001t0006g0010 others(2): Show |
5 | HG02015.hp2 NA18612.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1704C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000613 | |||||||
| chr4:39000629 | G | A | 1 | a0001c0001t0002g0347 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.89-1720C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000629 | |||||||
| chr4:39000650 | G | A | 47 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.89-1741C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000650 | |||||||
| chr4:39000652 | T | C | 123 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1743A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000652 | |||||||
| chr4:39000685 | G | A | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-1776C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000685 | |||||||
| chr4:39000757 | G | T | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-1848C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000757 | |||||||
| chr4:39000763 | T | C | 123 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1854A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000763 | |||||||
| chr4:39000814 | G | C | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1905C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000814 | |||||||
| chr4:39000880 | C | G | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1971G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000880 | |||||||
| chr4:39001013 | A | G | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2104T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001013 | |||||||
| chr4:39001128 | C | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0255 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2219G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001128 | |||||||
| chr4:39001128 | C | T | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2219G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001128 | |||||||
| chr4:39001179 | G | A | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-2270C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001179 | |||||||
| chr4:39001214 | C | CA | 31 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0091 others(28): Show |
31 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2306dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | |||||||
| chr4:39001214 | C | CAA | 67 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0036 others(64): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.89-2307_89-2306dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | |||||||
| chr4:39001214 | C | CAAA | 9 | a0001c0001t0001g0182 a0001c0001t0002g0108 a0001c0001t0003g0265 others(6): Show |
9 | HG02970.hp1 HG03130.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-2308_89-2306dup others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | |||||||
| chr4:39001214 | CA | C | 102 | a0001c0001t0001g0054 a0001c0001t0005g0248 a0001c0003t0002g0190 others(99): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.89-2306delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | |||||||
| chr4:39001280 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0004g0179 |
2 | NA18961.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.89-2371T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001280 | |||||||
| chr4:39001451 | A | C | 1 | a0001c0001t0009g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-2542T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001451 | |||||||
| chr4:39001538 | C | CT | 115 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.89-2630dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001538 | |||||||
| chr4:39001541 | C | CT | 47 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.89-2633dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001541 | |||||||
| chr4:39001541 | C | T | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2632G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001541 | |||||||
| chr4:39001544 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0003g0153 |
2 | NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.89-2635A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001544 | |||||||
| chr4:39001578 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0002g0068 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.89-2669T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001578 | |||||||
| chr4:39001630 | C | T | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2721G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001630 | |||||||
| chr4:39001634 | A | G | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.89-2725T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001634 | |||||||
| chr4:39001659 | A | G | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-2750T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001659 | |||||||
| chr4:39001712 | T | C | 120 | a0001c0001t0001g0054 a0001c0001t0005g0269 a0001c0001t0013g0266 others(117): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.89-2803A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001712 | |||||||
| chr4:39001728 | G | A | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2819C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001728 | |||||||
| chr4:39001733 | T | C | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-2824A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001733 | |||||||
| chr4:39001740 | C | G | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2831G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001740 | |||||||
| chr4:39001899 | T | C | 117 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(114): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.89-2990A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001899 | |||||||
| chr4:39001905 | C | T | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2996G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001905 | |||||||
| chr4:39001929 | C | A | 1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-3020G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001929 | |||||||
| chr4:39001969 | A | G | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3060T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001969 | |||||||
| chr4:39001989 | T | C | 187 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.89-3080A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001989 | |||||||
| chr4:39002018 | A | C | 190 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-3109T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002018 | |||||||
| chr4:39002170 | C | T | 5 | a0001c0001t0001g0237 a0001c0001t0002g0313 a0001c0001t0002g0314 others(2): Show |
5 | HG00544.hp2 HG03490.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3261G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002170 | |||||||
| chr4:39002219 | C | T | 6 | a0004c0005t0001g0133 a0004c0005t0001g0200 a0004c0005t0002g0254 others(3): Show |
6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002219 | |||||||
| chr4:39002220 | G | A | 1 | a0001c0001t0005g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.89-3311C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002220 | |||||||
| chr4:39002266 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.89-3357T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002266 | |||||||
| chr4:39002276 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002276 | |||||||
| chr4:39002382 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.89-3473G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002382 | |||||||
| chr4:39002383 | G | A | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3474C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002383 | |||||||
| chr4:39002449 | G | C | 5 | a0004c0005t0001g0200 a0004c0005t0002g0254 a0004c0005t0002g0258 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3540C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002449 | |||||||
| chr4:39002458 | T | C | 1 | a0004c0005t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-3549A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002458 | |||||||
| chr4:39002473 | C | T | 190 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-3564G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002473 | |||||||
| chr4:39002585 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3676C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002585 | |||||||
| chr4:39002597 | A | C | 189 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.89-3688T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002597 | |||||||
| chr4:39002683 | G | A | 10 | a0002c0002t0001g0210 a0002c0002t0002g0062 a0004c0005t0001g0200 others(7): Show |
10 | HG02055.hp1 HG02148.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-3774C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002683 | |||||||
| chr4:39002706 | A | C | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3797T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002706 | |||||||
| chr4:39002727 | T | C | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3818A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002727 | |||||||
| chr4:39002800 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-3891G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002800 | |||||||
| chr4:39002885 | G | C | 121 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.89-3976C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002885 | |||||||
| chr4:39002885 | G | T | 2 | a0001c0001t0005g0269 a0001c0001t0013g0266 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-3976C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002885 | |||||||
| chr4:39002939 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4030G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002939 | |||||||
| chr4:39002939 | C | T | 189 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.89-4030G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002939 | |||||||
| chr4:39002943 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.89-4034A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002943 | |||||||
| chr4:39002966 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0002g0158 |
2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.89-4057A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002966 | |||||||
| chr4:39003054 | G | A | 118 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-4145C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003054 | |||||||
| chr4:39003129 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.89-4220C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003129 | |||||||
| chr4:39003181 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.89-4272C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003181 | |||||||
| chr4:39003191 | T | A | 1 | a0002c0002t0001g0217 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.89-4282A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003191 | |||||||
| chr4:39003386 | G | A | 1 | a0001c0001t0004g0329 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.89-4477C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003386 | |||||||
| chr4:39003391 | G | A | 120 | a0001c0001t0001g0054 a0001c0001t0005g0269 a0001c0001t0013g0266 others(117): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.89-4482C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003391 | |||||||
| chr4:39003469 | G | A | 3 | a0006c0007t0001g0369 a0006c0007t0003g0288 a0006c0007t0006g0289 |
3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-4560C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003469 | |||||||
| chr4:39003522 | C | T | 117 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(114): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.89-4613G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003522 | |||||||
| chr4:39003576 | C | T | 3 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0015g0300 |
3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-4667G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003576 | |||||||
| chr4:39003585 | C | A | 1 | a0002c0002t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.89-4676G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003585 | |||||||
| chr4:39003652 | TA | T | 222 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.89-4744delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003652 | |||||||
| chr4:39003728 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.89-4819C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003728 | |||||||
| chr4:39003733 | T | G | 2 | a0001c0003t0001g0353 a0001c0003t0001g0367 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.89-4824A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003733 | |||||||
| chr4:39003740 | A | T | 2 | a0002c0002t0002g0160 a0002c0002t0005g0380 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.89-4831T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003740 | |||||||
| chr4:39003865 | A | G | 1 | a0001c0003t0004g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.89-4956T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003865 | |||||||
| chr4:39003879 | A | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0299 a0001c0001t0002g0301 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4970T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003879 | |||||||
| chr4:39003981 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.89-5072G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003981 | |||||||
| chr4:39004614 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-5705C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004614 | |||||||
| chr4:39004634 | T | A | 1 | a0002c0002t0001g0298 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.89-5725A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004634 | |||||||
| chr4:39004838 | A | G | 3 | a0001c0003t0002g0007 a0001c0003t0003g0105 a0001c0003t0004g0020 |
3 | NA18940.hp1 NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.89-5929T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004838 | |||||||
| chr4:39004925 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.89-6016G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004925 | |||||||
| chr4:39004995 | T | C | 1 | a0001c0001t0009g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-6086A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004995 | |||||||
| chr4:39005146 | C | T | 208 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.89-6237G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005146 | |||||||
| chr4:39005149 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.89-6240T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005149 | |||||||
| chr4:39005172 | G | C | 125 | a0001c0001t0001g0054 a0002c0002t0001g0019 a0002c0002t0001g0027 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-6263C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005172 | |||||||
| chr4:39005210 | G | A | 10 | a0002c0002t0001g0252 a0002c0002t0001g0253 a0002c0002t0001g0262 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-6301C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005210 | |||||||
| chr4:39005224 | G | A | 17 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0147 others(14): Show |
18 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-6315C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005224 | |||||||
| chr4:39005385 | C | A | 1 | a0002c0002t0001g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.89-6476G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005385 | |||||||
| chr4:39005532 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0002g0068 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.89-6623T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005532 | |||||||
| chr4:39005546 | G | A | 125 | a0001c0001t0001g0054 a0001c0001t0001g0299 a0001c0001t0002g0171 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-6637C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005546 | |||||||
| chr4:39005551 | G | T | 3 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0015g0300 |
3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-6642C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005551 | |||||||
| chr4:39005561 | AG | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(40): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-6653delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005561 | |||||||
| chr4:39005562 | G | A | 168 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0090 others(165): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.89-6653C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005562 | |||||||
| chr4:39005597 | AC | A | 6 | a0001c0001t0003g0265 a0001c0001t0005g0168 a0001c0001t0005g0251 others(3): Show |
6 | HG02970.hp1 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-6689delG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005597 | |||||||
| chr4:39005891 | G | A | 52 | a0001c0001t0001g0257 a0001c0001t0001g0291 a0001c0001t0002g0044 others(49): Show |
52 | HG00733.hp2 HG01891.hp2 HG01934.hp2 others(49): Show |
intron_variant | MODIFIER | c.89-6982C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005891 | |||||||
| chr4:39005895 | A | G | 1 | a0001c0003t0004g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.89-6986T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005895 | |||||||
| chr4:39005902 | C | A | 2 | a0001c0001t0001g0223 a0001c0001t0004g0224 |
2 | NA19009.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.89-6993G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005902 | |||||||
| chr4:39005964 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.89-7055G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005964 | |||||||
| chr4:39005981 | T | C | 206 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.89-7072A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005981 | |||||||
| chr4:39006033 | T | C | 1 | a0001c0003t0002g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.89-7124A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006033 | |||||||
| chr4:39006047 | C | T | 4 | a0004c0005t0001g0200 a0004c0005t0003g0201 a0006c0007t0003g0288 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-7138G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006047 | |||||||
| chr4:39006159 | G | C | 1 | a0001c0001t0005g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89-7250C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006159 | |||||||
| chr4:39006162 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-7253G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006162 | |||||||
| chr4:39006372 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.89-7463G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006372 | |||||||
| chr4:39006472 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-7563C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006472 | |||||||
| chr4:39006485 | T | C | 16 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(13): Show |
16 | HG00099.hp1 HG01168.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-7576A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006485 | |||||||
| chr4:39006495 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.89-7586T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006495 | |||||||
| chr4:39006630 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.89-7721C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006630 | |||||||
| chr4:39006633 | C | A | 3 | a0001c0001t0002g0028 a0001c0001t0005g0269 a0001c0001t0005g0290 |
3 | HG02615.hp1 HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7724G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006633 | |||||||
| chr4:39006657 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.89-7748G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006657 | |||||||
| chr4:39006812 | G | A | 1 | a0001c0009t0001g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-7903C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006812 | |||||||
| chr4:39006881 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0005g0290 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7972G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006881 | |||||||
| chr4:39006962 | A | C | 3 | a0001c0001t0001g0295 a0001c0001t0002g0296 a0001c0001t0005g0161 |
3 | HG02145.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.89-8053T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006962 | |||||||
| chr4:39007031 | C | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0102 others(100): Show |
104 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.89-8122G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007031 | |||||||
| chr4:39007066 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.89-8157G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007066 | |||||||
| chr4:39007113 | T | C | 4 | a0001c0001t0009g0376 a0006c0007t0001g0369 a0006c0007t0003g0288 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-8204A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007113 | |||||||
| chr4:39007173 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(148): Show |
152 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.89-8264C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007173 | |||||||
| chr4:39007185 | C | G | 128 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.89-8276G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007185 | |||||||
| chr4:39007201 | T | C | 5 | a0001c0001t0005g0248 a0002c0002t0001g0252 a0002c0002t0001g0253 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-8292A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007201 | |||||||
| chr4:39007236 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.89-8327C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007236 | |||||||
| chr4:39007345 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0002g0268 a0001c0001t0008g0063 |
4 | HG01167.hp2 HG01169.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8436C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007345 | |||||||
| chr4:39007415 | T | TTTTATTT others(1): Show |
50 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(47): Show |
50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-8514_89-8507dup others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007415 | |||||||
| chr4:39007701 | C | A | 11 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-8792G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007701 | |||||||
| chr4:39007720 | G | T | 2 | a0004c0005t0002g0254 a0004c0005t0002g0258 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.89-8811C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007720 | |||||||
| chr4:39007811 | T | A | 3 | a0001c0001t0001g0306 a0001c0001t0002g0137 a0002c0002t0002g0095 |
3 | NA19058.hp1 NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.89-8902A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007811 | |||||||
| chr4:39007897 | T | C | 50 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(47): Show |
50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-8988A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007897 | |||||||
| chr4:39007945 | T | A | 27 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-9036A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007945 | |||||||
| chr4:39008133 | T | G | 1 | a0001c0001t0004g0081 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.89-9224A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008133 | |||||||
| chr4:39008219 | C | T | 1 | a0001c0001t0005g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-9310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008219 | |||||||
| chr4:39008233 | T | G | 1 | a0001c0001t0004g0331 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.89-9324A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008233 | |||||||
| chr4:39008348 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0002g0124 a0001c0001t0004g0009 others(22): Show |
27 | HG00609.hp1 HG02071.hp2 NA18747.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-9439G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008348 | |||||||
| chr4:39008360 | T | C | 35 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-9451A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008360 | |||||||
| chr4:39008602 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0008g0063 |
3 | HG01167.hp2 HG01169.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.89-9693C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008602 | |||||||
| chr4:39008625 | T | C | 35 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-9716A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008625 | |||||||
| chr4:39008632 | C | T | 38 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0157 others(35): Show |
38 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-9723G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008632 | |||||||
| chr4:39008756 | A | G | 2 | a0001c0001t0005g0168 a0004c0005t0001g0133 |
2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.89-9847T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008756 | |||||||
| chr4:39008790 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-9881G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008790 | |||||||
| chr4:39009258 | A | G | 50 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(47): Show |
50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-10349T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009258 | |||||||
| chr4:39009351 | A | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.89-10442T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009351 | |||||||
| chr4:39009475 | G | A | 2 | a0004c0005t0002g0254 a0004c0005t0002g0258 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.89-10566C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009475 | |||||||
| chr4:39009490 | A | T | 1 | a0001c0001t0003g0377 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.89-10581T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009490 | |||||||
| chr4:39009669 | C | T | 1 | a0001c0001t0005g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.89-10760G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009669 | |||||||
| chr4:39009696 | A | G | 50 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(47): Show |
50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-10787T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009696 | |||||||
| chr4:39009862 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.89-10953T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009862 | |||||||
| chr4:39010207 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0307 others(6): Show |
9 | HG01192.hp1 HG01261.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-11298A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010207 | |||||||
| chr4:39010220 | A | G | 1 | a0002c0002t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.89-11311T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010220 | |||||||
| chr4:39010289 | G | A | 15 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(12): Show |
15 | HG00099.hp1 HG01168.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.89-11380C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010289 | |||||||
| chr4:39010887 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(319): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.89-11978G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010887 | |||||||
| chr4:39011010 | T | C | 41 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0149 others(38): Show |
41 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-12101A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011010 | |||||||
| chr4:39011277 | G | A | 27 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-12368C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011277 | |||||||
| chr4:39011354 | C | A | 3 | a0001c0001t0001g0247 a0001c0001t0002g0199 a0004c0005t0005g0249 |
3 | HG02622.hp1 HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.89-12445G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011354 | |||||||
| chr4:39011368 | G | A | 14 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0246 others(11): Show |
14 | HG01255.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-12459C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011368 | |||||||
| chr4:39011399 | A | G | 4 | a0001c0001t0009g0376 a0006c0007t0001g0369 a0006c0007t0003g0288 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-12490T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011399 | |||||||
| chr4:39011449 | T | TA | 27 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-12541dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011449 | |||||||
| chr4:39011644 | A | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(304): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.89-12735T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011644 | |||||||
| chr4:39011646 | G | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.89-12737C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011646 | |||||||
| chr4:39011666 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-12757G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011666 | |||||||
| chr4:39011704 | C | T | 1 | a0001c0001t0005g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-12795G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011704 | |||||||
| chr4:39011705 | G | A | 35 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-12796C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011705 | |||||||
| chr4:39011756 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0003g0056 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.89-12847C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011756 | |||||||
| chr4:39011899 | G | T | 1 | a0001c0001t0001g0358 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-12990C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011899 | |||||||
| chr4:39012025 | G | T | 5 | a0001c0001t0005g0290 a0001c0001t0009g0376 a0006c0007t0001g0369 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-13116C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012025 | |||||||
| chr4:39012029 | G | A | 1 | a0002c0002t0002g0213 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-13120C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012029 | |||||||
| chr4:39012113 | G | A | 1 | a0001c0001t0005g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-13204C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012113 | |||||||
| chr4:39012123 | A | G | 2 | a0001c0001t0005g0168 a0004c0005t0001g0133 |
2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.89-13214T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012123 | |||||||
| chr4:39012169 | T | A | 1 | a0002c0002t0004g0113 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.89-13260A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012169 | |||||||
| chr4:39012172 | A | T | 1 | a0002c0002t0004g0113 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.89-13263T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012172 | |||||||
| chr4:39012193 | A | G | 5 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0001g0239 others(2): Show |
5 | HG00621.hp2 NA19000.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-13284T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012193 | |||||||
| chr4:39012275 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.89-13366T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012275 | |||||||
| chr4:39012624 | G | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(181): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.89-13715C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012624 | |||||||
| chr4:39012673 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.89-13764C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012673 | |||||||
| chr4:39012714 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(181): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.89-13805G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012714 | |||||||
| chr4:39012738 | G | A | 1 | a0002c0002t0002g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.89-13829C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012738 | |||||||
| chr4:39012948 | A | G | 1 | a0001c0001t0003g0094 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.89-14039T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012948 | |||||||
| chr4:39012995 | G | T | 38 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0157 others(35): Show |
38 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-14086C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012995 | |||||||
| chr4:39013098 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.89-14189G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013098 | |||||||
| chr4:39013133 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.89-14224A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013133 | |||||||
| chr4:39013307 | CA | C | 127 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(124): Show |
127 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-14399delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013307 | |||||||
| chr4:39013320 | AG | A | 4 | a0001c0001t0009g0376 a0006c0007t0001g0369 a0006c0007t0003g0288 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-14412delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013320 | |||||||
| chr4:39013321 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-14412C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013321 | |||||||
| chr4:39013325 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-14416C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013325 | |||||||
| chr4:39013362 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.89-14453A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013362 | |||||||
| chr4:39013373 | GTTTA | G | 89 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0086 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.89-14468_89-14465d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013373 | GTTTATTT others(1): Show |
G | 165 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(162): Show |
167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.89-14472_89-14465d others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013373 | GTTTATTT others(5): Show |
G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0109 others(73): Show |
77 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.89-14476_89-14465d others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013373 | GTTTATTT others(9): Show |
G | 33 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(30): Show |
33 | HG01192.hp1 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-14480_89-14465d others(18): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013373 | GTTTATTT others(13): Show |
G | 6 | a0001c0001t0002g0163 a0001c0001t0005g0040 a0001c0001t0009g0376 others(3): Show |
6 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-14484_89-14465d others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013373 | GTTTATTT others(17): Show |
G | 1 | a0001c0001t0004g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.89-14488_89-14465d others(26): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | |||||||
| chr4:39013481 | A | AC | 195 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(192): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.89-14573dupG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013481 | |||||||
| chr4:39013589 | C | T | 4 | a0001c0001t0009g0376 a0006c0007t0001g0369 a0006c0007t0003g0288 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-14680G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013589 | |||||||
| chr4:39013652 | G | A | 35 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-14743C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013652 | |||||||
| chr4:39013990 | C | G | 2 | a0001c0001t0001g0295 a0001c0001t0002g0296 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.89-15081G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013990 | |||||||
| chr4:39014146 | A | C | 27 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0091 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-15237T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014146 | |||||||
| chr4:39014225 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0002g0309 |
2 | HG01168.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.89-15316G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014225 | |||||||
| chr4:39014380 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-15471T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014380 | |||||||
| chr4:39014455 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.89-15546A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014455 | |||||||
| chr4:39014570 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-15661G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014570 | |||||||
| chr4:39014591 | T | A | 35 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(32): Show |
35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-15682A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014591 | |||||||
| chr4:39014650 | CG | C | 11 | a0001c0001t0001g0162 a0001c0001t0001g0371 a0001c0001t0001g0374 others(8): Show |
11 | HG02615.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-15742delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014650 | |||||||
| chr4:39014655 | G | C | 5 | a0002c0002t0001g0031 a0002c0002t0001g0110 a0002c0002t0003g0088 others(2): Show |
5 | NA18939.hp1 NA18948.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-15746C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014655 | |||||||
| chr4:39014757 | CA | C | 114 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(111): Show |
114 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.89-15849delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014757 | |||||||
| chr4:39014757 | CAA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(179): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.89-15850_89-15849d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014757 | |||||||
| chr4:39015171 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-16262C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015171 | |||||||
| chr4:39015272 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.89-16363C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015272 | |||||||
| chr4:39015408 | T | C | 2 | a0001c0001t0003g0192 a0002c0002t0001g0191 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.89-16499A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015408 | |||||||
| chr4:39015575 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88+16651G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015575 | |||||||
| chr4:39015580 | G | C | 1 | a0002c0002t0003g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.88+16646C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015580 | |||||||
| chr4:39015632 | A | T | 2 | a0001c0001t0001g0275 a0002c0002t0007g0308 |
2 | NA18966.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.88+16594T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015632 | |||||||
| chr4:39015914 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+16312G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015914 | |||||||
| chr4:39016223 | A | C | 49 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0164 others(46): Show |
49 | HG01109.hp2 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.88+16003T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016223 | |||||||
| chr4:39016263 | C | T | 7 | a0001c0001t0001g0371 a0001c0001t0001g0374 a0001c0001t0001g0375 others(4): Show |
7 | HG02647.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+15963G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016263 | |||||||
| chr4:39016298 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(97): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.88+15928C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016298 | |||||||
| chr4:39016371 | T | TA | 62 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0140 others(59): Show |
62 | HG00323.hp1 HG00423.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.88+15854dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016371 | |||||||
| chr4:39016383 | AAAG | A | 18 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0188 others(15): Show |
18 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+15840_88+15842d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016383 | |||||||
| chr4:39016385 | AG | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0044 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+15840delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016385 | |||||||
| chr4:39016386 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(181): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.88+15840C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016386 | |||||||
| chr4:39016387 | A | AC | 7 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0003g0192 others(4): Show |
7 | HG01243.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+15838_88+15839i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016387 | |||||||
| chr4:39016387 | A | C | 55 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0059 others(52): Show |
55 | HG00280.hp1 HG00639.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+15839T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016387 | |||||||
| chr4:39016752 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0044 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+15474A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016752 | |||||||
| chr4:39016771 | T | C | 1 | a0002c0002t0002g0357 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.88+15455A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016771 | |||||||
| chr4:39016840 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+15386G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016840 | |||||||
| chr4:39016842 | G | A | 44 | a0001c0001t0001g0164 a0001c0001t0001g0169 a0001c0001t0001g0245 others(41): Show |
44 | HG01109.hp2 HG01168.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.88+15384C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016842 | |||||||
| chr4:39017018 | A | G | 2 | a0002c0002t0001g0027 a0002c0002t0001g0053 |
2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.88+15208T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017018 | |||||||
| chr4:39017171 | C | CTT | 8 | a0001c0001t0001g0112 a0001c0001t0001g0140 a0001c0001t0001g0246 others(5): Show |
8 | HG01168.hp2 HG01175.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+15053_88+15054d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | |||||||
| chr4:39017171 | C | CTTT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.88+15052_88+15054d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | |||||||
| chr4:39017171 | C | CTTTT | 29 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0047 others(26): Show |
29 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.88+15051_88+15054d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | |||||||
| chr4:39017171 | CT | C | 39 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0223 others(36): Show |
39 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.88+15054delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | |||||||
| chr4:39017202 | T | C | 3 | a0001c0001t0001g0162 a0004c0005t0001g0200 a0004c0005t0003g0201 |
3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15024A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017202 | |||||||
| chr4:39017203 | C | G | 3 | a0001c0001t0001g0162 a0004c0005t0001g0200 a0004c0005t0003g0201 |
3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15023G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017203 | |||||||
| chr4:39017204 | T | A | 3 | a0001c0001t0001g0162 a0004c0005t0001g0200 a0004c0005t0003g0201 |
3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15022A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017204 | |||||||
| chr4:39017205 | C | G | 3 | a0001c0001t0001g0162 a0004c0005t0001g0200 a0004c0005t0003g0201 |
3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15021G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017205 | |||||||
| chr4:39017205 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+15021G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017205 | |||||||
| chr4:39017206 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0003g0242 a0004c0005t0001g0200 others(1): Show |
4 | HG02055.hp1 HG02602.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+15020C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017206 | |||||||
| chr4:39017299 | C | T | 5 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(2): Show |
5 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+14927G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017299 | |||||||
| chr4:39017324 | G | A | 9 | a0001c0001t0001g0169 a0001c0001t0002g0171 a0001c0001t0003g0173 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+14902C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017324 | |||||||
| chr4:39017332 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.88+14894C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017332 | |||||||
| chr4:39017340 | AATTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0359 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.88+14875_88+14885d others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017340 | |||||||
| chr4:39017713 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0002g0115 |
2 | NA19005.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.88+14513A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017713 | |||||||
| chr4:39017963 | A | T | 5 | a0001c0001t0001g0154 a0001c0001t0003g0150 a0001c0001t0003g0153 others(2): Show |
5 | HG02015.hp1 NA18951.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14263T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017963 | |||||||
| chr4:39018032 | G | C | 5 | a0001c0001t0001g0162 a0001c0001t0004g0159 a0001c0001t0004g0195 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14194C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018032 | |||||||
| chr4:39018257 | T | C | 57 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0169 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.88+13969A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018257 | |||||||
| chr4:39018267 | C | A | 7 | a0001c0001t0001g0371 a0001c0001t0001g0374 a0001c0001t0001g0375 others(4): Show |
7 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+13959G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018267 | |||||||
| chr4:39018292 | G | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(218): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.88+13934C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018292 | |||||||
| chr4:39018294 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(218): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.88+13932A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018294 | |||||||
| chr4:39018340 | T | C | 2 | a0001c0001t0003g0192 a0002c0002t0001g0191 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.88+13886A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018340 | |||||||
| chr4:39018574 | T | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(152): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.88+13652A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018574 | |||||||
| chr4:39018629 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.88+13597G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018629 | |||||||
| chr4:39018677 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+13549T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018677 | |||||||
| chr4:39018709 | C | A | 2 | a0004c0005t0001g0200 a0004c0005t0003g0201 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+13517G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018709 | |||||||
| chr4:39018805 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.88+13421A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018805 | |||||||
| chr4:39018842 | G | T | 24 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(21): Show |
24 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.88+13384C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018842 | |||||||
| chr4:39018855 | T | C | 2 | a0004c0005t0001g0200 a0004c0005t0003g0201 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+13371A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018855 | |||||||
| chr4:39018893 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+13333G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018893 | |||||||
| chr4:39018978 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+13248C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018978 | |||||||
| chr4:39018996 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.88+13230C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018996 | |||||||
| chr4:39019023 | AAAAAC | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0169 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+13198_88+13202d others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019023 | |||||||
| chr4:39019024 | AAAAC | A | 46 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(43): Show |
46 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.88+13198_88+13201d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019024 | |||||||
| chr4:39019025 | AAAC | A | 16 | a0001c0001t0001g0182 a0001c0001t0002g0163 a0001c0001t0002g0260 others(13): Show |
16 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+13198_88+13200d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019025 | |||||||
| chr4:39019026 | AACAAAAC | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(142): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.88+13193_88+13199d others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019026 | |||||||
| chr4:39019033 | C | A | 70 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0157 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.88+13193G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | |||||||
| chr4:39019033 | C | CA | 7 | a0001c0001t0001g0364 a0001c0001t0002g0189 a0001c0001t0004g0360 others(4): Show |
7 | HG00621.hp1 HG01361.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+13192dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | |||||||
| chr4:39019033 | C | G | 2 | a0001c0001t0002g0115 a0001c0003t0004g0020 |
2 | NA18940.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.88+13193G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | |||||||
| chr4:39019034 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(138): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.88+13192T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019034 | |||||||
| chr4:39019035 | A | G | 1 | a0002c0002t0006g0014 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.88+13191T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019035 | |||||||
| chr4:39019038 | A | C | 15 | a0001c0001t0001g0121 a0001c0001t0001g0139 a0001c0001t0001g0371 others(12): Show |
15 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.88+13188T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019038 | |||||||
| chr4:39019039 | A | C | 2 | a0001c0001t0001g0295 a0001c0001t0002g0296 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88+13187T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019039 | |||||||
| chr4:39019041 | A | C | 2 | a0004c0005t0002g0254 a0004c0005t0002g0258 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.88+13185T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019041 | |||||||
| chr4:39019050 | C | A | 4 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+13176G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019050 | |||||||
| chr4:39019133 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+13093C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019133 | |||||||
| chr4:39019271 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0004g0009 a0001c0001t0006g0010 others(1): Show |
4 | NA18943.hp1 NA18972.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+12955A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019271 | |||||||
| chr4:39019299 | T | C | 2 | a0001c0001t0001g0117 a0002c0002t0001g0116 |
2 | HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.88+12927A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019299 | |||||||
| chr4:39019405 | T | C | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+12821A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019405 | |||||||
| chr4:39019497 | C | T | 4 | a0001c0001t0002g0189 a0001c0003t0001g0186 a0001c0003t0002g0187 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+12729G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019497 | |||||||
| chr4:39019700 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(151): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.88+12526A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019700 | |||||||
| chr4:39019920 | T | C | 1 | a0004c0005t0002g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+12306A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019920 | |||||||
| chr4:39020025 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0004g0159 a0001c0001t0004g0195 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+12201T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020025 | |||||||
| chr4:39020125 | A | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(269): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.88+12101T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020125 | |||||||
| chr4:39020142 | T | C | 1 | a0001c0001t0005g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+12084A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020142 | |||||||
| chr4:39020226 | T | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0044 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+12000A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020226 | |||||||
| chr4:39020290 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(198): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.88+11936G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020290 | |||||||
| chr4:39020359 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.88+11867G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020359 | |||||||
| chr4:39020461 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.88+11765G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020461 | |||||||
| chr4:39020490 | C | A | 8 | a0001c0001t0001g0371 a0001c0001t0001g0374 a0001c0001t0001g0375 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+11736G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020490 | |||||||
| chr4:39020648 | C | A | 2 | a0001c0001t0002g0378 a0001c0001t0005g0379 |
2 | HG01167.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.88+11578G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020648 | |||||||
| chr4:39020659 | C | A | 11 | a0001c0001t0002g0124 a0002c0002t0001g0019 a0002c0002t0002g0003 others(8): Show |
12 | HG00609.hp1 HG02071.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+11567G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020659 | |||||||
| chr4:39020675 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+11551C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020675 | |||||||
| chr4:39020705 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.88+11521T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020705 | |||||||
| chr4:39020895 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(212): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.88+11331A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020895 | |||||||
| chr4:39020913 | C | T | 3 | a0001c0001t0004g0159 a0001c0001t0004g0195 a0002c0002t0002g0160 |
3 | HG02258.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88+11313G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020913 | |||||||
| chr4:39020920 | G | A | 1 | a0001c0001t0006g0010 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.88+11306C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020920 | |||||||
| chr4:39021009 | A | G | 1 | a0002c0002t0003g0381 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.88+11217T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021009 | |||||||
| chr4:39021059 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.88+11167G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021059 | |||||||
| chr4:39021075 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+11151A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021075 | |||||||
| chr4:39021139 | A | T | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+11087T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021139 | |||||||
| chr4:39021232 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.88+10994C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021232 | |||||||
| chr4:39021394 | C | CA | 266 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.88+10831dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021394 | |||||||
| chr4:39021412 | T | A | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+10814A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021412 | |||||||
| chr4:39021416 | A | T | 1 | a0001c0001t0005g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+10810T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021416 | |||||||
| chr4:39021436 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.88+10790A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021436 | |||||||
| chr4:39021592 | G | A | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(3): Show |
6 | NA18957.hp1 NA18961.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+10634C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021592 | |||||||
| chr4:39021827 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+10399G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021827 | |||||||
| chr4:39021946 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+10280G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021946 | |||||||
| chr4:39021982 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+10244G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021982 | |||||||
| chr4:39022079 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(152): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.88+10147A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022079 | |||||||
| chr4:39022093 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.88+10133A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022093 | |||||||
| chr4:39022200 | T | C | 4 | a0002c0002t0001g0236 a0002c0002t0002g0233 a0002c0002t0004g0234 others(1): Show |
4 | HG02738.hp2 NA18942.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10026A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022200 | |||||||
| chr4:39022372 | C | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.88+9854G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022372 | |||||||
| chr4:39022901 | GA | G | 4 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0009g0302 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9324delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022901 | |||||||
| chr4:39022911 | C | G | 4 | a0001c0001t0001g0299 a0001c0001t0002g0301 a0001c0001t0009g0302 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9315G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022911 | |||||||
| chr4:39023068 | A | T | 1 | a0002c0002t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+9158T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023068 | |||||||
| chr4:39023353 | A | G | 99 | a0001c0001t0001g0149 a0001c0001t0001g0162 a0001c0001t0001g0164 others(96): Show |
99 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.88+8873T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023353 | |||||||
| chr4:39023401 | A | G | 4 | a0001c0001t0005g0248 a0002c0002t0001g0252 a0002c0002t0001g0253 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+8825T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023401 | |||||||
| chr4:39023766 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(152): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.88+8460T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023766 | |||||||
| chr4:39023851 | T | C | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+8375A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023851 | |||||||
| chr4:39023885 | C | A | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+8341G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023885 | |||||||
| chr4:39024180 | C | T | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+8046G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024180 | |||||||
| chr4:39024224 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(267): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+8002A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024224 | |||||||
| chr4:39024334 | C | A | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7892G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024334 | |||||||
| chr4:39024397 | C | T | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7829G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024397 | |||||||
| chr4:39024432 | A | T | 8 | a0001c0001t0001g0371 a0001c0001t0001g0374 a0001c0001t0001g0375 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+7794T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024432 | |||||||
| chr4:39024721 | A | G | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7505T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024721 | |||||||
| chr4:39025076 | C | T | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+7150G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025076 | |||||||
| chr4:39025113 | C | A | 2 | a0001c0001t0001g0157 a0001c0001t0002g0158 |
2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.88+7113G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025113 | |||||||
| chr4:39025138 | C | T | 1 | a0001c0001t0005g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.88+7088G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025138 | |||||||
| chr4:39025206 | A | G | 374 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(371): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.88+7020T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025206 | |||||||
| chr4:39025210 | G | C | 59 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0169 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.88+7016C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025210 | |||||||
| chr4:39025250 | C | A | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+6976G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025250 | |||||||
| chr4:39025264 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+6962G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025264 | |||||||
| chr4:39025315 | T | C | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+6911A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025315 | |||||||
| chr4:39025345 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(141): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.88+6880dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | |||||||
| chr4:39025345 | C | CAA | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0135 others(15): Show |
18 | HG01123.hp1 HG01361.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.88+6879_88+6880dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | |||||||
| chr4:39025345 | CA | C | 46 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(43): Show |
46 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.88+6880delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | |||||||
| chr4:39025462 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(152): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.88+6764A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025462 | |||||||
| chr4:39025521 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88+6705C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025521 | |||||||
| chr4:39025617 | G | A | 2 | a0002c0002t0002g0382 a0002c0002t0003g0381 |
2 | HG00673.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.88+6609C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025617 | |||||||
| chr4:39025656 | G | A | 2 | a0001c0001t0003g0004 a0002c0002t0001g0155 |
3 | HG01069.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.88+6570C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025656 | |||||||
| chr4:39025656 | G | C | 1 | a0001c0001t0013g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.88+6570C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025656 | |||||||
| chr4:39025657 | G | T | 1 | a0001c0001t0004g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.88+6569C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025657 | |||||||
| chr4:39025684 | T | G | 5 | a0001c0001t0001g0162 a0001c0001t0004g0159 a0001c0001t0004g0195 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+6542A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025684 | |||||||
| chr4:39025718 | T | C | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+6508A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025718 | |||||||
| chr4:39025815 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0026 others(6): Show |
9 | HG01123.hp1 HG01433.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6411G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025815 | |||||||
| chr4:39026053 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.88+6173T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026053 | |||||||
| chr4:39026081 | T | G | 1 | a0001c0001t0001g0368 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.88+6145A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026081 | |||||||
| chr4:39026128 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88+6098A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026128 | |||||||
| chr4:39026358 | T | A | 2 | a0001c0001t0001g0162 a0001c0001t0005g0161 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.88+5868A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026358 | |||||||
| chr4:39026365 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88+5861T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026365 | |||||||
| chr4:39026369 | A | T | 2 | a0001c0001t0001g0295 a0001c0001t0002g0296 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88+5857T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026369 | |||||||
| chr4:39026377 | A | AG | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+5848_88+5849ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026377 | |||||||
| chr4:39026378 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+5848T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026378 | |||||||
| chr4:39026570 | T | C | 50 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0154 others(47): Show |
50 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.88+5656A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026570 | |||||||
| chr4:39026612 | A | G | 2 | a0001c0001t0002g0293 a0002c0002t0003g0294 |
2 | HG02135.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.88+5614T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026612 | |||||||
| chr4:39026698 | G | A | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+5528C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026698 | |||||||
| chr4:39026787 | C | T | 2 | a0001c0001t0003g0192 a0002c0002t0001g0191 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.88+5439G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026787 | |||||||
| chr4:39026798 | G | A | 43 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(40): Show |
43 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.88+5428C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026798 | |||||||
| chr4:39026820 | G | A | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+5406C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026820 | |||||||
| chr4:39027004 | T | G | 8 | a0001c0001t0001g0371 a0001c0001t0001g0374 a0001c0001t0001g0375 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+5222A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027004 | |||||||
| chr4:39027025 | C | T | 1 | a0001c0003t0004g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.88+5201G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027025 | |||||||
| chr4:39027211 | T | C | 1 | a0002c0002t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88+5015A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027211 | |||||||
| chr4:39027436 | G | T | 48 | a0001c0001t0001g0154 a0001c0001t0001g0207 a0001c0001t0001g0208 others(45): Show |
48 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+4790C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027436 | |||||||
| chr4:39027548 | T | G | 1 | a0002c0002t0003g0365 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.88+4678A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027548 | |||||||
| chr4:39027551 | C | CT | 22 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0278 others(19): Show |
22 | HG00733.hp1 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.88+4674dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | |||||||
| chr4:39027551 | CT | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0021 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.88+4674delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | |||||||
| chr4:39027551 | CTT | C | 17 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0184 others(14): Show |
17 | HG01169.hp1 HG01255.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+4673_88+4674del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | |||||||
| chr4:39027758 | C | CT | 13 | a0001c0001t0001g0162 a0001c0001t0001g0196 a0001c0001t0002g0197 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+4467dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027758 | |||||||
| chr4:39027758 | C | CTT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(146): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.88+4466_88+4467dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027758 | |||||||
| chr4:39027761 | T | TC | 55 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0169 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.88+4464_88+4465ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027761 | |||||||
| chr4:39027762 | T | C | 2 | a0001c0001t0004g0194 a0001c0003t0002g0190 |
2 | HG01169.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.88+4464A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027762 | |||||||
| chr4:39027764 | T | C | 1 | a0001c0001t0001g0368 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.88+4462A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027764 | |||||||
| chr4:39027849 | T | C | 49 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0207 others(46): Show |
49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+4377A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027849 | |||||||
| chr4:39028016 | C | CA | 49 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0207 others(46): Show |
49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+4209dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028016 | |||||||
| chr4:39028020 | G | A | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+4206C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028020 | |||||||
| chr4:39028077 | G | A | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+4149C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028077 | |||||||
| chr4:39028153 | T | A | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+4073A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028153 | |||||||
| chr4:39028306 | A | G | 1 | a0006c0007t0001g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.88+3920T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028306 | |||||||
| chr4:39028563 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+3663T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028563 | |||||||
| chr4:39028820 | A | G | 50 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0207 others(47): Show |
50 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.88+3406T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028820 | |||||||
| chr4:39028872 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.88+3354T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028872 | |||||||
| chr4:39029058 | A | G | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG00323.hp1 HG01243.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+3168T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029058 | |||||||
| chr4:39029157 | T | C | 49 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0207 others(46): Show |
49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+3069A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029157 | |||||||
| chr4:39029420 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0270 |
2 | HG02273.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.88+2806T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029420 | |||||||
| chr4:39029456 | TAAGAACT others(275): Show |
T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(274): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.88+2488_88+2769del | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029456 | |||||||
| chr4:39029524 | C | T | 1 | a0001c0001t0003g0325 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.88+2702G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029524 | |||||||
| chr4:39029545 | T | C | 1 | a0001c0003t0003g0351 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.88+2681A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029545 | |||||||
| chr4:39029596 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.88+2630G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029596 | |||||||
| chr4:39029713 | C | CA | 38 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0279 others(35): Show |
38 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.88+2512dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029713 | |||||||
| chr4:39029757 | A | C | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+2469T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029757 | |||||||
| chr4:39029764 | C | A | 5 | a0001c0001t0001g0188 a0001c0001t0002g0189 a0001c0003t0001g0186 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+2462G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029764 | |||||||
| chr4:39029972 | T | C | 47 | a0001c0001t0001g0154 a0001c0001t0001g0207 a0001c0001t0001g0208 others(44): Show |
47 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.88+2254A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029972 | |||||||
| chr4:39030179 | T | TA | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+2046dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030179 | |||||||
| chr4:39030179 | T | TAA | 8 | a0001c0001t0002g0241 a0001c0001t0003g0192 a0001c0001t0003g0242 others(5): Show |
8 | HG00423.hp2 HG00621.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+2045_88+2046dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030179 | |||||||
| chr4:39030193 | C | A | 42 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(39): Show |
42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+2033G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030193 | |||||||
| chr4:39030222 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+2004G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030222 | |||||||
| chr4:39030289 | G | T | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0008g0244 others(1): Show |
4 | HG01255.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1937C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030289 | |||||||
| chr4:39030359 | C | T | 42 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(39): Show |
42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+1867G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030359 | |||||||
| chr4:39030481 | C | T | 6 | a0001c0001t0001g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+1745G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030481 | |||||||
| chr4:39030565 | A | T | 1 | a0002c0002t0005g0380 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+1661T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030565 | |||||||
| chr4:39030723 | G | A | 59 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0169 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.88+1503C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030723 | |||||||
| chr4:39030747 | C | A | 42 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(39): Show |
42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+1479G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030747 | |||||||
| chr4:39030952 | G | C | 1 | a0001c0001t0004g0194 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.88+1274C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030952 | |||||||
| chr4:39031403 | T | A | 1 | a0001c0001t0004g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+823A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031403 | |||||||
| chr4:39031469 | T | C | 1 | a0001c0001t0004g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+757A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031469 | |||||||
| chr4:39031572 | A | G | 64 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+654T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031572 | |||||||
| chr4:39031761 | G | A | 2 | a0001c0001t0002g0378 a0001c0001t0005g0379 |
2 | HG01167.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.88+465C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031761 | |||||||
| chr4:39031782 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0004g0009 a0001c0001t0006g0010 others(1): Show |
4 | NA18943.hp1 NA18972.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+444G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031782 | |||||||
| chr4:39031875 | T | A | 2 | a0001c0001t0003g0004 a0002c0002t0001g0155 |
3 | HG01069.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.88+351A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031875 | |||||||
| chr4:39031887 | AAAAT | A | 25 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(22): Show |
25 | HG01168.hp1 HG01255.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.88+335_88+338delAT others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031887 | |||||||
| chr4:39031888 | AAAT | A | 37 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0157 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.88+335_88+337delAT others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031888 | |||||||
| chr4:39031889 | AAT | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(178): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.88+335_88+336delAT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031889 | |||||||
| chr4:39031890 | AT | A | 24 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0058 others(21): Show |
24 | HG01175.hp1 HG01346.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.88+335delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031890 | |||||||
| chr4:39031891 | T | A | 2 | a0001c0001t0001g0114 a0002c0002t0005g0380 |
2 | HG03195.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.88+335A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031891 | |||||||
| chr4:39031894 | A | T | 2 | a0001c0001t0002g0268 a0001c0001t0005g0269 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.88+332T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031894 | |||||||
| chr4:39031898 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+328A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031898 | |||||||
| chr4:39031902 | A | C | 2 | a0001c0001t0001g0157 a0001c0001t0002g0158 |
2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.88+324T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031902 | |||||||
| chr4:39031904 | A | C | 1 | a0001c0003t0002g0007 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.88+322T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031904 | |||||||
| chr4:39031905 | A | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.88+321T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031905 | |||||||
| chr4:39031913 | A | AT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(153): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.88+312_88+313insA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031913 | |||||||
| chr4:39032117 | T | A | 2 | a0002c0002t0002g0382 a0002c0002t0003g0381 |
2 | HG00673.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.88+109A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39032117 | |||||||
| chr4:39032186 | A | T | 1 | a0002c0002t0004g0006 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.88+40T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39032186 |