Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 219623 |
| ensemblid | ENSG00000196932.12 |
| hgncid | 28550 |
| symbol | TMEM26 |
| name | transmembrane protein 26 |
| refseq_nuc | NM_178505.8 |
| refseq_prot | NP_848600.2 |
| ensembl_nuc | ENST00000399298.8 |
| ensembl_prot | ENSP00000382237.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 61406642 |
| end | 61453381 |
| strand | - |
| ver | v1.2 |
| region | chr10:61406642-61453381 |
| region5000 | chr10:61401642-61458381 |
| regionname0 | TMEM26_chr10_61406642_61453381 |
| regionname5000 | TMEM26_chr10_61401642_61458381 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 368 | 353 | 88 | 65 | 150 | 12 | 36 | 124 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(363): Show |
chr10 | 61401642 | 61458381 |
| a0002 | 0/0 | 368 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(363): Show |
chr10 | 61401642 | 61458381 |
| a0003 | 0/0 | 61 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(56): Show |
chr10 | 61401642 | 61458381 |
| a0004 | 0/0 | 368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(363): Show |
chr10 | 61401642 | 61458381 |
| a0005 | 0/0 | 368 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(363): Show |
chr10 | 61401642 | 61458381 |
| a0006 | 0/0 | 368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | MEGLV others(363): Show |
chr10 | 61401642 | 61458381 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1104 | 284 | 51 | 57 | 132 | 9 | 33 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0001c0002 | 0/0 | 1104 | 69 | 37 | 8 | 18 | 3 | 3 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0002c0003 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0003c0004 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0004c0005 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0005c0007 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 | ||
| a0006c0006 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | ATGGA others(1099): Show |
chr10 | 61401642 | 61458381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5087 | 130 | 16 | 32 | 58 | 6 | 16 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0002 | 0/0 | 5087 | 70 | 3 | 10 | 48 | 3 | 6 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0003 | 0/0 | 5087 | 34 | 20 | 5 | 6 | 0 | 3 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0006 | 0/0 | 5087 | 9 | 0 | 3 | 4 | 0 | 2 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0007 | 0/0 | 5088 | 5 | 0 | 0 | 4 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5083): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0008 | 0/0 | 5087 | 5 | 3 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0010 | 0/0 | 5087 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0014 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0015 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0018 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0019 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0020 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0022 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0023 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0024 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0025 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0026 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0027 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0028 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0029 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0030 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0031 | 0/0 | 5088 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5083): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0032 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0033 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0034 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0035 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0036 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0037 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0038 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0039 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0041 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0043 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0001t0046 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0004 | 0/0 | 5087 | 27 | 6 | 1 | 16 | 2 | 2 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0005 | 0/0 | 5087 | 20 | 18 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0009 | 0/0 | 5087 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0011 | 0/0 | 5087 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0012 | 0/0 | 5087 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0013 | 0/0 | 5087 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0016 | 0/0 | 5087 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0017 | 0/0 | 5087 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0040 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0042 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0044 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0001c0002t0045 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0002c0003t0006 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0003c0004t0021 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0004c0005t0003 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0005c0007t0001 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| a0006c0006t0003 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | AGCGC others(5082): Show |
chr10 | 61401642 | 61458381 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 2 | 0 | 11 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 2 | 3 | 2 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0008g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0008g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0010g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0014g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0015g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0019g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0022g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0023g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0024g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0025g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0026g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0027g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0028g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0029g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0030g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0031g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0032g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0033g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0034g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0035g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0036g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0037g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0038g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0039g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0041g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0043g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0001t0046g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0009g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0012g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0012g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0013g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0013g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0017g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0017g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0040g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0042g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0044g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0001c0002t0045g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0002c0003t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0003c0004t0021g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0004c0005t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0005c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| a0006c0006t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00323 | hp1 | a0001 | c0002 | t0004 | g0255 | EUR | FIN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0257 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00544 | hp1 | a0001 | c0001 | t0027 | g0117 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0232 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00673 | hp1 | a0001 | c0001 | t0022 | g0129 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00735 | hp2 | a0001 | c0001 | t0037 | g0078 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00738 | hp1 | a0001 | c0002 | t0012 | g0163 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01070 | hp2 | a0001 | c0001 | t0018 | g0046 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01071 | hp1 | a0001 | c0002 | t0040 | g0100 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01081 | hp1 | a0001 | c0002 | t0017 | g0264 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0043 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01192 | hp2 | a0001 | c0001 | t0039 | g0221 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0044 | AMR | PUR | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0039 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01346 | hp1 | a0001 | c0001 | t0033 | g0116 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01433 | hp1 | a0001 | c0002 | t0016 | g0235 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01433 | hp2 | a0002 | c0003 | t0006 | g0048 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01515 | hp1 | a0001 | c0002 | t0017 | g0252 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0192 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0226 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02004 | hp1 | a0001 | c0001 | t0026 | g0112 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02055 | hp1 | a0001 | c0002 | t0009 | g0160 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02056 | hp2 | a0001 | c0002 | t0042 | g0250 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02083 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02135 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0240 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0043 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02293 | hp1 | a0001 | c0002 | t0012 | g0164 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0236 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0222 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0241 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0249 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02630 | hp1 | a0001 | c0001 | t0043 | g0270 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02630 | hp2 | a0001 | c0002 | t0013 | g0242 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0266 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02683 | hp2 | a0003 | c0004 | t0021 | g0049 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0268 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0044 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02723 | hp2 | a0001 | c0002 | t0044 | g0244 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0040 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0045 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02818 | hp2 | a0001 | c0001 | t0025 | g0142 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02886 | hp2 | a0001 | c0002 | t0009 | g0161 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0045 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02895 | hp2 | a0001 | c0002 | t0011 | g0066 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02896 | hp2 | a0001 | c0002 | t0009 | g0030 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0263 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0261 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02922 | hp2 | a0004 | c0005 | t0003 | g0158 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02965 | hp1 | a0001 | c0002 | t0009 | g0030 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02965 | hp2 | a0001 | c0001 | t0034 | g0152 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02970 | hp2 | a0001 | c0001 | t0028 | g0224 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0041 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0021 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0239 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0272 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0271 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03098 | hp2 | a0001 | c0001 | t0035 | g0050 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03195 | hp2 | a0001 | c0001 | t0020 | g0134 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03209 | hp1 | a0001 | c0002 | t0009 | g0162 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0267 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0269 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0238 | AFR | ESN | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0041 | AFR | GWD | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03579 | hp1 | a0001 | c0002 | t0013 | g0245 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0262 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03654 | hp2 | a0001 | c0001 | t0046 | g0273 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03669 | hp1 | a0001 | c0002 | t0045 | g0253 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03669 | hp2 | a0005 | c0007 | t0001 | g0102 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0233 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0014 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03704 | hp2 | a0001 | c0001 | t0019 | g0047 | SAS | PJL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0054 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03927 | hp1 | a0001 | c0001 | t0038 | g0213 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0021 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0040 | AFR | YRI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18522 | hp2 | a0001 | c0002 | t0011 | g0166 | AFR | YRI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18612 | hp1 | a0001 | c0002 | t0012 | g0159 | EAS | CHB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0256 | EAS | CHB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18941 | hp1 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18942 | hp1 | a0001 | c0001 | t0030 | g0081 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18954 | hp2 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0246 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18967 | hp2 | a0001 | c0001 | t0015 | g0022 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18993 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18998 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19004 | hp2 | a0001 | c0001 | t0031 | g0091 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19011 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19012 | hp1 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19043 | hp1 | a0001 | c0001 | t0036 | g0153 | AFR | LWK | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0237 | AFR | LWK | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19060 | hp1 | a0001 | c0001 | t0032 | g0085 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0022 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19064 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19074 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19079 | hp1 | a0001 | c0001 | t0014 | g0118 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19083 | hp2 | a0001 | c0001 | t0014 | g0113 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0247 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20129 | hp1 | a0001 | c0002 | t0013 | g0243 | AFR | ASW | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ASW | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0251 | EUR | TSI | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20905 | hp1 | a0001 | c0001 | t0041 | g0228 | SAS | GIH | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | GIH | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0165 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG03471 | hp2 | a0001 | c0002 | t0016 | g0265 | AFR | MSL | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0170 | AFR | USA | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | USA | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA21309 | hp1 | a0006 | c0006 | t0003 | g0182 | AFR | LWK | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| NA21309 | hp2 | a0001 | c0001 | t0029 | g0067 | AFR | LWK | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0025 | REF | REF | TMEM26_chr10_61401642_61458381 | TMEM26 | chr10 | 61401642 | 61458381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:61410378 | C | G | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1051G>C | p.Ala351Pro | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1351/5087 | 1051/1107 | 351/368 | chr10 | 61410378 | |||
| chr10:61410453 | G | A | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.976C>T | p.His326Tyr | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1276/5087 | 976/1107 | 326/368 | chr10 | 61410453 | |||
| chr10:61431220 | G | A | 1 | a0005 | 1 | HG03669.hp2 | missense_variant&splice_region_variant | MODERATE | c.383C>T | p.Thr128Met | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/6 | 683/5087 | 383/1107 | 128/368 | chr10 | 61431220 | |||
| chr10:61452896 | G | T | 1 | a0003 | 1 | HG02683.hp2 | stop_gained | HIGH | c.186C>A | p.Tyr62* | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 486/5087 | 186/1107 | 62/368 | chr10 | 61452896 | |||
| chr10:61452916 | A | G | 1 | a0002 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.166T>C | p.Phe56Leu | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 466/5087 | 166/1107 | 56/368 | chr10 | 61452916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:61410534 | A | G | 1 | a0001c0002 | 69 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(66): Show |
synonymous_variant | LOW | c.895T>C | p.Leu299Leu | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1195/5087 | 895/1107 | 299/368 | chr10 | 61410534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:61406688 | C | G | 1 | a0001c0002t0045 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3634G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3634 | chr10 | 61406688 | ||||||
| chr10:61406903 | C | T | 1 | a0001c0001t0030 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3419G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3419 | chr10 | 61406903 | ||||||
| chr10:61406967 | G | GA | 2 | a0001c0001t0007 a0001c0001t0031 |
6 | HG00609.hp1 HG03688.hp1 NA18978.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3354dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3354 | chr10 | 61406967 | ||||||
| chr10:61407015 | G | A | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(25): Show |
192 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3307C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3307 | chr10 | 61407015 | ||||||
| chr10:61407075 | C | T | 1 | a0001c0001t0029 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3247G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3247 | chr10 | 61407075 | ||||||
| chr10:61407114 | T | C | 2 | a0001c0001t0023 a0001c0001t0028 |
2 | HG02451.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3208A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3208 | chr10 | 61407114 | ||||||
| chr10:61407115 | C | T | 2 | a0001c0001t0023 a0001c0001t0028 |
2 | HG02451.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3207G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3207 | chr10 | 61407115 | ||||||
| chr10:61407168 | A | G | 1 | a0001c0002t0012 | 3 | HG00738.hp1 HG02293.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3154T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3154 | chr10 | 61407168 | ||||||
| chr10:61407257 | T | C | 1 | a0001c0001t0008 | 5 | HG01070.hp1 HG01071.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3065A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3065 | chr10 | 61407257 | ||||||
| chr10:61407278 | G | A | 1 | a0001c0001t0032 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3044C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 3044 | chr10 | 61407278 | ||||||
| chr10:61407374 | G | A | 13 | a0001c0001t0025 a0001c0001t0034 a0001c0002t0004 others(10): Show |
69 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2948C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2948 | chr10 | 61407374 | ||||||
| chr10:61407504 | T | C | 8 | a0001c0001t0034 a0001c0002t0004 a0001c0002t0013 others(5): Show |
37 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2818A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2818 | chr10 | 61407504 | ||||||
| chr10:61407576 | G | A | 1 | a0001c0001t0035 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2746C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2746 | chr10 | 61407576 | ||||||
| chr10:61407595 | G | A | 1 | a0001c0001t0033 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2727 | chr10 | 61407595 | ||||||
| chr10:61407646 | A | G | 12 | a0001c0001t0025 a0001c0001t0034 a0001c0002t0004 others(9): Show |
63 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2676T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2676 | chr10 | 61407646 | ||||||
| chr10:61407650 | G | A | 1 | a0001c0001t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2672C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2672 | chr10 | 61407650 | ||||||
| chr10:61407930 | G | C | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(30): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2392C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2392 | chr10 | 61407930 | ||||||
| chr10:61408086 | A | G | 2 | a0001c0001t0023 a0001c0001t0028 |
2 | HG02451.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2236T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2236 | chr10 | 61408086 | ||||||
| chr10:61408198 | G | A | 1 | a0001c0002t0013 | 3 | HG02630.hp2 HG03579.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2124C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2124 | chr10 | 61408198 | ||||||
| chr10:61408226 | G | A | 1 | a0001c0001t0037 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2096 | chr10 | 61408226 | ||||||
| chr10:61408245 | C | T | 1 | a0001c0001t0027 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2077 | chr10 | 61408245 | ||||||
| chr10:61408259 | A | G | 1 | a0001c0001t0026 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 2063 | chr10 | 61408259 | ||||||
| chr10:61408564 | A | G | 1 | a0001c0001t0010 | 3 | NA18979.hp2 NA18998.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1758T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1758 | chr10 | 61408564 | ||||||
| chr10:61408730 | A | G | 11 | a0001c0001t0025 a0001c0002t0004 a0001c0002t0005 others(8): Show |
62 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1592T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1592 | chr10 | 61408730 | ||||||
| chr10:61408769 | A | C | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1553T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1553 | chr10 | 61408769 | ||||||
| chr10:61408803 | C | T | 1 | a0001c0002t0016 | 2 | HG01433.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1519G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1519 | chr10 | 61408803 | ||||||
| chr10:61408809 | A | C | 1 | a0001c0001t0023 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1513 | chr10 | 61408809 | ||||||
| chr10:61409052 | G | A | 1 | a0001c0001t0038 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1270C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1270 | chr10 | 61409052 | ||||||
| chr10:61409222 | G | A | 1 | a0001c0001t0039 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1100C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1100 | chr10 | 61409222 | ||||||
| chr10:61409261 | C | T | 1 | a0001c0001t0022 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1061G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 1061 | chr10 | 61409261 | ||||||
| chr10:61409390 | A | C | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0018 others(3): Show |
41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*932T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 932 | chr10 | 61409390 | ||||||
| chr10:61409641 | T | C | 1 | a0001c0001t0014 | 2 | NA19079.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*681A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 681 | chr10 | 61409641 | ||||||
| chr10:61409751 | G | T | 1 | a0001c0002t0009 | 5 | HG02055.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*571C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 571 | chr10 | 61409751 | ||||||
| chr10:61409822 | G | A | 1 | a0001c0001t0015 | 2 | NA18967.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*500C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 500 | chr10 | 61409822 | ||||||
| chr10:61409895 | C | T | 1 | a0003c0004t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 427 | chr10 | 61409895 | ||||||
| chr10:61410106 | C | T | 1 | a0001c0002t0044 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 216 | chr10 | 61410106 | ||||||
| chr10:61410138 | T | C | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0018 others(3): Show |
41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*184A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 184 | chr10 | 61410138 | ||||||
| chr10:61410193 | T | A | 12 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0009 others(9): Show |
69 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*129A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 129 | chr10 | 61410193 | ||||||
| chr10:61410236 | C | T | 1 | a0001c0001t0020 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*86G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 86 | chr10 | 61410236 | ||||||
| chr10:61410299 | C | A | 1 | a0001c0001t0041 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 23 | chr10 | 61410299 | ||||||
| chr10:61410300 | G | T | 1 | a0001c0002t0042 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 6/6 | 22 | chr10 | 61410300 | ||||||
| chr10:61453127 | G | T | 1 | a0001c0001t0019 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 46 | chr10 | 61453127 | ||||||
| chr10:61453196 | T | C | 9 | a0001c0001t0043 a0001c0002t0004 a0001c0002t0005 others(6): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
5_prime_UTR_variant | MODIFIER | c.-115A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 115 | chr10 | 61453196 | ||||||
| chr10:61453253 | C | T | 1 | a0001c0001t0018 | 1 | HG01070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-172G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 172 | chr10 | 61453253 | ||||||
| chr10:61453287 | G | A | 1 | a0001c0001t0046 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/6 | 206 | chr10 | 61453287 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:61410774 | A | C | 1 | a0001c0001t0001g0017 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.683-28T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61410774 | |||||||
| chr10:61410801 | G | A | 1 | a0001c0001t0001g0023 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.683-55C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61410801 | |||||||
| chr10:61411022 | C | A | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.683-276G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411022 | |||||||
| chr10:61411074 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.683-328T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411074 | |||||||
| chr10:61411079 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.683-333C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411079 | |||||||
| chr10:61411176 | T | C | 1 | a0001c0002t0004g0255 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.683-430A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411176 | |||||||
| chr10:61411183 | C | T | 2 | a0001c0002t0004g0251 a0001c0002t0004g0255 |
2 | HG00323.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.683-437G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411183 | |||||||
| chr10:61411230 | G | A | 3 | a0001c0001t0003g0033 a0001c0001t0003g0175 a0001c0001t0003g0183 |
4 | HG01884.hp2 HG02109.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-484C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411230 | |||||||
| chr10:61411310 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.683-564A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411310 | |||||||
| chr10:61411329 | C | A | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.683-583G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411329 | |||||||
| chr10:61411498 | T | C | 1 | a0001c0001t0006g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.683-752A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411498 | |||||||
| chr10:61411665 | T | G | 1 | a0001c0001t0002g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.683-919A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411665 | |||||||
| chr10:61411666 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.683-920A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411666 | |||||||
| chr10:61411813 | G | T | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.683-1067C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411813 | |||||||
| chr10:61411818 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0131 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.683-1072G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61411818 | |||||||
| chr10:61412160 | C | G | 2 | a0001c0001t0034g0152 a0001c0001t0036g0153 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.682+1299G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412160 | |||||||
| chr10:61412248 | C | CTG | 5 | a0001c0001t0001g0093 a0001c0001t0001g0132 a0001c0001t0020g0134 others(2): Show |
5 | HG00544.hp2 HG02895.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1209_682+1210d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412248 | |||||||
| chr10:61412248 | C | CTGTG | 8 | a0001c0001t0002g0151 a0001c0001t0008g0032 a0001c0001t0008g0040 others(5): Show |
10 | HG01070.hp1 HG01071.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+1207_682+1210d others(6): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412248 | |||||||
| chr10:61412248 | CTG | C | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1209_682+1210d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412248 | |||||||
| chr10:61412314 | C | T | 1 | a0001c0001t0035g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.682+1145G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412314 | |||||||
| chr10:61412376 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.682+1083T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412376 | |||||||
| chr10:61412398 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.682+1061G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412398 | |||||||
| chr10:61412410 | A | T | 33 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(30): Show |
43 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.682+1049T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412410 | |||||||
| chr10:61412460 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.682+999A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412460 | |||||||
| chr10:61412658 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.682+801A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412658 | |||||||
| chr10:61412766 | T | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+693A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412766 | |||||||
| chr10:61412799 | C | T | 1 | a0001c0001t0025g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.682+660G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412799 | |||||||
| chr10:61412800 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+659C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412800 | |||||||
| chr10:61412812 | G | A | 1 | a0001c0001t0007g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.682+647C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412812 | |||||||
| chr10:61412936 | A | G | 49 | a0001c0001t0001g0206 a0001c0001t0002g0002 a0001c0001t0002g0003 others(46): Show |
71 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+523T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412936 | |||||||
| chr10:61412992 | C | CATGGGTC others(33): Show |
9 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(6): Show |
11 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+427_682+466dup others(40): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61412992 | |||||||
| chr10:61413181 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+278C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61413181 | |||||||
| chr10:61413181 | G | T | 33 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(30): Show |
43 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.682+278C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61413181 | |||||||
| chr10:61413184 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.682+275C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61413184 | |||||||
| chr10:61413208 | C | T | 90 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(87): Show |
122 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.682+251G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 5/5 | chr10 | 61413208 | |||||||
| chr10:61413547 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG00642.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-12T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61413547 | |||||||
| chr10:61413554 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.606-19C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61413554 | |||||||
| chr10:61413639 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.606-104C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61413639 | |||||||
| chr10:61413680 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.606-145A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61413680 | |||||||
| chr10:61413863 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02602.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.606-328C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61413863 | |||||||
| chr10:61414047 | A | G | 3 | a0001c0001t0003g0033 a0001c0001t0003g0175 a0001c0001t0003g0183 |
4 | HG01884.hp2 HG02109.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-512T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414047 | |||||||
| chr10:61414278 | G | T | 2 | a0001c0001t0003g0187 a0001c0001t0018g0046 |
2 | HG01070.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.606-743C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414278 | |||||||
| chr10:61414436 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.606-901T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414436 | |||||||
| chr10:61414548 | C | A | 9 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(6): Show |
11 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.606-1013G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414548 | |||||||
| chr10:61414797 | C | T | 12 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(9): Show |
16 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.606-1262G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414797 | |||||||
| chr10:61414832 | T | A | 1 | a0001c0001t0034g0152 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.606-1297A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414832 | |||||||
| chr10:61414848 | G | C | 1 | a0001c0001t0002g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.606-1313C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61414848 | |||||||
| chr10:61415002 | G | A | 1 | a0001c0002t0040g0100 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.606-1467C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415002 | |||||||
| chr10:61415052 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.606-1517T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415052 | |||||||
| chr10:61415107 | C | A | 56 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(53): Show |
69 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.606-1572G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415107 | |||||||
| chr10:61415328 | T | A | 33 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(30): Show |
43 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.606-1793A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415328 | |||||||
| chr10:61415395 | G | T | 1 | a0001c0002t0005g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.606-1860C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415395 | |||||||
| chr10:61415413 | T | A | 1 | a0003c0004t0021g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.606-1878A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415413 | |||||||
| chr10:61415799 | T | C | 55 | a0001c0001t0001g0206 a0001c0001t0002g0002 a0001c0001t0002g0003 others(52): Show |
77 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.606-2264A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415799 | |||||||
| chr10:61415814 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.606-2279C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415814 | |||||||
| chr10:61415919 | A | T | 20 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0042 others(17): Show |
25 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.606-2384T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415919 | |||||||
| chr10:61415950 | T | C | 2 | a0001c0001t0002g0151 a0001c0001t0025g0142 |
2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.606-2415A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61415950 | |||||||
| chr10:61416036 | G | A | 90 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(87): Show |
122 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.606-2501C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416036 | |||||||
| chr10:61416059 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.606-2524T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416059 | |||||||
| chr10:61416071 | G | T | 1 | a0001c0001t0003g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.606-2536C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416071 | |||||||
| chr10:61416075 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0025g0142 |
2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.606-2540G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416075 | |||||||
| chr10:61416570 | A | C | 1 | a0001c0001t0039g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.606-3035T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416570 | |||||||
| chr10:61416647 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0039g0221 |
2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.606-3112T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416647 | |||||||
| chr10:61416699 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.606-3164G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416699 | |||||||
| chr10:61416769 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.606-3234G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416769 | |||||||
| chr10:61416950 | C | T | 37 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(34): Show |
47 | HG00609.hp1 HG00639.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.606-3415G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416950 | |||||||
| chr10:61416951 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.606-3416C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416951 | |||||||
| chr10:61416963 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606-3428C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61416963 | |||||||
| chr10:61417102 | T | A | 2 | a0001c0002t0004g0254 a0001c0002t0004g0260 |
2 | NA18941.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.606-3567A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417102 | |||||||
| chr10:61417139 | G | A | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.606-3604C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417139 | |||||||
| chr10:61417232 | C | A | 162 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(159): Show |
211 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.606-3697G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417232 | |||||||
| chr10:61417465 | G | GT | 51 | a0001c0001t0001g0098 a0001c0001t0001g0206 a0001c0001t0002g0002 others(48): Show |
75 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.606-3931dupA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417465 | |||||||
| chr10:61417465 | GT | G | 21 | a0001c0001t0001g0123 a0001c0001t0003g0181 a0001c0001t0025g0142 others(18): Show |
26 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.606-3931delA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417465 | |||||||
| chr10:61417488 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-3953T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417488 | |||||||
| chr10:61417495 | C | T | 1 | a0001c0001t0003g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.606-3960G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417495 | |||||||
| chr10:61417656 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.606-4121C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417656 | |||||||
| chr10:61417923 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-4388T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61417923 | |||||||
| chr10:61418072 | AT | A | 5 | a0001c0001t0002g0151 a0001c0001t0025g0142 a0001c0001t0034g0152 others(2): Show |
5 | HG02818.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.606-4538delA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418072 | |||||||
| chr10:61418142 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.606-4607C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418142 | |||||||
| chr10:61418233 | C | T | 55 | a0001c0001t0001g0206 a0001c0001t0002g0002 a0001c0001t0002g0003 others(52): Show |
77 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.606-4698G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418233 | |||||||
| chr10:61418248 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-4713A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418248 | |||||||
| chr10:61418387 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-4852A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418387 | |||||||
| chr10:61418396 | T | C | 1 | a0001c0002t0011g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.606-4861A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418396 | |||||||
| chr10:61418396 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-4861A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418396 | |||||||
| chr10:61418525 | C | CA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0084 others(6): Show |
10 | HG00408.hp2 HG01496.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-4991dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418525 | |||||||
| chr10:61418538 | A | G | 1 | a0001c0001t0003g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.606-5003T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418538 | |||||||
| chr10:61418553 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5018A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418553 | |||||||
| chr10:61418557 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5022A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418557 | |||||||
| chr10:61418582 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5047A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418582 | |||||||
| chr10:61418637 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.606-5102T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418637 | |||||||
| chr10:61418751 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0124 |
2 | HG01358.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.606-5216A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418751 | |||||||
| chr10:61418815 | T | C | 33 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(30): Show |
43 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.606-5280A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418815 | |||||||
| chr10:61418833 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5298T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418833 | |||||||
| chr10:61418834 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5299C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61418834 | |||||||
| chr10:61419080 | A | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0203 |
2 | HG01255.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.606-5545T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419080 | |||||||
| chr10:61419111 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5576T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419111 | |||||||
| chr10:61419183 | G | A | 1 | a0001c0001t0036g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606-5648C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419183 | |||||||
| chr10:61419191 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.606-5656G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419191 | |||||||
| chr10:61419403 | G | T | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.606-5868C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419403 | |||||||
| chr10:61419427 | G | T | 11 | a0001c0002t0005g0041 a0001c0002t0005g0043 a0001c0002t0005g0044 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.606-5892C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419427 | |||||||
| chr10:61419456 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5921A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419456 | |||||||
| chr10:61419494 | A | C | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-5959T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419494 | |||||||
| chr10:61419522 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-5987T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419522 | |||||||
| chr10:61419531 | G | GA | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-5997dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419531 | |||||||
| chr10:61419659 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-6124A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419659 | |||||||
| chr10:61419711 | T | C | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.606-6176A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419711 | |||||||
| chr10:61419778 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-6243T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419778 | |||||||
| chr10:61419848 | T | A | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-6313A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419848 | |||||||
| chr10:61419882 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.606-6347G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61419882 | |||||||
| chr10:61420082 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.606-6547G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420082 | |||||||
| chr10:61420104 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.606-6569T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420104 | |||||||
| chr10:61420131 | T | C | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-6596A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420131 | |||||||
| chr10:61420136 | T | G | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6601A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420136 | |||||||
| chr10:61420137 | A | T | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6602T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420137 | |||||||
| chr10:61420140 | T | A | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6605A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420140 | |||||||
| chr10:61420141 | G | T | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6606C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420141 | |||||||
| chr10:61420143 | A | T | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6608T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420143 | |||||||
| chr10:61420144 | T | G | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.606-6609A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420144 | |||||||
| chr10:61420224 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-6689A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420224 | |||||||
| chr10:61420278 | T | C | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-6743A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420278 | |||||||
| chr10:61420391 | G | A | 1 | a0001c0001t0007g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.606-6856C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420391 | |||||||
| chr10:61420431 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0169 others(1): Show |
5 | HG00597.hp1 NA18967.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.606-6896G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420431 | |||||||
| chr10:61420432 | G | A | 1 | a0001c0001t0039g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.606-6897C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420432 | |||||||
| chr10:61420547 | T | C | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.606-7012A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420547 | |||||||
| chr10:61420549 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.606-7014A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420549 | |||||||
| chr10:61420631 | T | TTA | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-7098_606-7097d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420631 | |||||||
| chr10:61420659 | AATAATTC others(3): Show |
A | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-7134_606-7125d others(12): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420659 | |||||||
| chr10:61420670 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-7135T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420670 | |||||||
| chr10:61420723 | T | TA | 6 | a0001c0001t0001g0076 a0001c0001t0001g0084 a0001c0001t0001g0101 others(3): Show |
6 | HG02451.hp2 NA18992.hp1 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-7189dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420723 | |||||||
| chr10:61420723 | TAAA | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.606-7191_606-7189d others(5): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420723 | |||||||
| chr10:61420795 | A | T | 1 | a0001c0001t0003g0130 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.606-7260T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420795 | |||||||
| chr10:61420800 | G | A | 48 | a0001c0001t0002g0013 a0001c0001t0002g0208 a0001c0001t0043g0270 others(45): Show |
62 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.606-7265C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420800 | |||||||
| chr10:61420853 | A | G | 2 | a0001c0002t0009g0030 a0001c0002t0009g0160 |
3 | HG02055.hp1 HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.606-7318T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420853 | |||||||
| chr10:61420935 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.606-7400G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420935 | |||||||
| chr10:61420959 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.606-7424T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420959 | |||||||
| chr10:61420993 | A | G | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.606-7458T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61420993 | |||||||
| chr10:61421018 | A | T | 4 | a0001c0002t0005g0237 a0001c0002t0005g0238 a0001c0002t0005g0241 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-7483T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421018 | |||||||
| chr10:61421037 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-7502T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421037 | |||||||
| chr10:61421115 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.606-7580G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421115 | |||||||
| chr10:61421128 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606-7593C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421128 | |||||||
| chr10:61421202 | T | A | 1 | a0001c0002t0012g0164 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.606-7667A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421202 | |||||||
| chr10:61421260 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(267): Show |
354 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(351): Show |
intron_variant | MODIFIER | c.605+7666A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421260 | |||||||
| chr10:61421333 | T | C | 1 | a0001c0001t0025g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.605+7593A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421333 | |||||||
| chr10:61421431 | T | C | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.605+7495A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421431 | |||||||
| chr10:61421505 | G | A | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.605+7421C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421505 | |||||||
| chr10:61421605 | T | C | 2 | a0001c0001t0003g0143 a0001c0001t0003g0144 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.605+7321A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421605 | |||||||
| chr10:61421672 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.605+7254T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421672 | |||||||
| chr10:61421677 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.605+7249G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421677 | |||||||
| chr10:61421769 | G | T | 1 | a0001c0002t0005g0041 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.605+7157C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421769 | |||||||
| chr10:61421987 | T | C | 26 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0236 others(23): Show |
33 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.605+6939A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61421987 | |||||||
| chr10:61422077 | C | T | 1 | a0001c0002t0009g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.605+6849G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422077 | |||||||
| chr10:61422304 | G | T | 1 | a0001c0001t0003g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.605+6622C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422304 | |||||||
| chr10:61422399 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.605+6527A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422399 | |||||||
| chr10:61422577 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.605+6349C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422577 | |||||||
| chr10:61422736 | CA | C | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+6189delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422736 | |||||||
| chr10:61422775 | A | G | 3 | a0001c0001t0003g0177 a0001c0001t0003g0180 a0001c0001t0003g0181 |
3 | HG00639.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.605+6151T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422775 | |||||||
| chr10:61422934 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.605+5992T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422934 | |||||||
| chr10:61422980 | A | C | 1 | a0001c0002t0042g0250 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.605+5946T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61422980 | |||||||
| chr10:61423159 | A | T | 1 | a0001c0001t0002g0097 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.605+5767T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423159 | |||||||
| chr10:61423189 | T | G | 3 | a0001c0001t0002g0036 a0001c0001t0002g0192 a0001c0001t0002g0209 |
4 | HG00741.hp1 HG01361.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+5737A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423189 | |||||||
| chr10:61423199 | A | G | 20 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0042 others(17): Show |
25 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.605+5727T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423199 | |||||||
| chr10:61423377 | T | C | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+5549A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423377 | |||||||
| chr10:61423597 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.605+5329G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423597 | |||||||
| chr10:61423708 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.605+5218C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423708 | |||||||
| chr10:61423719 | C | A | 2 | a0001c0002t0009g0161 a0004c0005t0003g0158 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.605+5207G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423719 | |||||||
| chr10:61423820 | G | A | 3 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
3 | NA18950.hp2 NA18990.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.605+5106C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423820 | |||||||
| chr10:61423825 | C | A | 145 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(142): Show |
191 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.605+5101G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423825 | |||||||
| chr10:61423862 | A | C | 1 | a0001c0001t0002g0208 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.605+5064T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61423862 | |||||||
| chr10:61424230 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.605+4696T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424230 | |||||||
| chr10:61424281 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.605+4645A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424281 | |||||||
| chr10:61424362 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0089 others(1): Show |
6 | HG00544.hp2 NA18978.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.605+4564C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424362 | |||||||
| chr10:61424696 | C | T | 12 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(9): Show |
15 | HG00597.hp1 HG00609.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.605+4230G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424696 | |||||||
| chr10:61424729 | A | C | 2 | a0001c0002t0013g0243 a0001c0002t0013g0245 |
2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.605+4197T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424729 | |||||||
| chr10:61424752 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.605+4174G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424752 | |||||||
| chr10:61424780 | C | T | 13 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(10): Show |
15 | HG00408.hp1 HG00609.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.605+4146G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424780 | |||||||
| chr10:61424781 | G | A | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.605+4145C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61424781 | |||||||
| chr10:61425090 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.605+3836G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425090 | |||||||
| chr10:61425133 | G | A | 3 | a0001c0001t0003g0130 a0001c0001t0003g0146 a0001c0001t0003g0147 |
3 | NA18956.hp1 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.605+3793C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425133 | |||||||
| chr10:61425176 | G | A | 3 | a0001c0001t0020g0134 a0001c0001t0029g0067 a0001c0002t0011g0066 |
3 | HG02895.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.605+3750C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425176 | |||||||
| chr10:61425189 | T | C | 9 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(6): Show |
11 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.605+3737A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425189 | |||||||
| chr10:61425198 | G | C | 27 | a0001c0002t0004g0006 a0001c0002t0004g0014 a0001c0002t0004g0015 others(24): Show |
35 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.605+3728C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425198 | |||||||
| chr10:61425239 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.605+3687G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425239 | |||||||
| chr10:61425337 | C | A | 1 | a0001c0001t0035g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.605+3589G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425337 | |||||||
| chr10:61425489 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.605+3437G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425489 | |||||||
| chr10:61425520 | G | C | 1 | a0001c0002t0004g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.605+3406C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425520 | |||||||
| chr10:61425718 | C | G | 2 | a0001c0001t0003g0187 a0001c0001t0018g0046 |
2 | HG01070.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.605+3208G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425718 | |||||||
| chr10:61425763 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.605+3163C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425763 | |||||||
| chr10:61425904 | A | G | 4 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0011g0165 others(1): Show |
5 | HG02055.hp1 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.605+3022T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425904 | |||||||
| chr10:61425984 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.605+2942T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61425984 | |||||||
| chr10:61426021 | A | G | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.605+2905T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426021 | |||||||
| chr10:61426049 | A | G | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.605+2877T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426049 | |||||||
| chr10:61426367 | C | T | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.605+2559G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426367 | |||||||
| chr10:61426385 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.605+2541A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426385 | |||||||
| chr10:61426435 | G | A | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.605+2491C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426435 | |||||||
| chr10:61426650 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.605+2276T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426650 | |||||||
| chr10:61426884 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.605+2042G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426884 | |||||||
| chr10:61426928 | G | A | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.605+1998C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426928 | |||||||
| chr10:61426985 | A | T | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.605+1941T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61426985 | |||||||
| chr10:61427054 | G | A | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.605+1872C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427054 | |||||||
| chr10:61427085 | T | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
6 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.605+1841A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427085 | |||||||
| chr10:61427345 | C | T | 10 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0009g0161 others(7): Show |
11 | HG00738.hp1 HG02055.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.605+1581G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427345 | |||||||
| chr10:61427409 | A | G | 3 | a0001c0001t0020g0134 a0001c0001t0029g0067 a0001c0002t0011g0066 |
3 | HG02895.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.605+1517T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427409 | |||||||
| chr10:61427444 | A | C | 2 | a0001c0002t0009g0161 a0004c0005t0003g0158 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.605+1482T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427444 | |||||||
| chr10:61427522 | A | G | 1 | a0001c0002t0016g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.605+1404T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427522 | |||||||
| chr10:61427540 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.605+1386G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427540 | |||||||
| chr10:61427732 | G | A | 145 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(142): Show |
191 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.605+1194C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427732 | |||||||
| chr10:61427837 | A | C | 1 | a0001c0001t0002g0200 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.605+1089T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427837 | |||||||
| chr10:61427890 | A | T | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.605+1036T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427890 | |||||||
| chr10:61427901 | C | T | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.605+1025G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427901 | |||||||
| chr10:61427947 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.605+979A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61427947 | |||||||
| chr10:61428304 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.605+622A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61428304 | |||||||
| chr10:61428542 | G | C | 9 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(6): Show |
11 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.605+384C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61428542 | |||||||
| chr10:61428553 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.605+373A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61428553 | |||||||
| chr10:61428819 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0084 a0001c0001t0001g0105 others(3): Show |
7 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.605+107T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 4/5 | chr10 | 61428819 | |||||||
| chr10:61429183 | G | A | 11 | a0001c0002t0005g0041 a0001c0002t0005g0043 a0001c0002t0005g0044 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-37C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429183 | |||||||
| chr10:61429195 | G | A | 2 | a0001c0002t0004g0254 a0001c0002t0004g0260 |
2 | NA18941.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.385-49C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429195 | |||||||
| chr10:61429294 | C | G | 1 | a0001c0001t0029g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385-148G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429294 | |||||||
| chr10:61429505 | T | A | 45 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0002 others(42): Show |
66 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.385-359A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429505 | |||||||
| chr10:61429530 | TTTTC | T | 10 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0009g0161 others(7): Show |
11 | HG00738.hp1 HG02055.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-388_385-385del others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429530 | |||||||
| chr10:61429559 | G | A | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.385-413C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429559 | |||||||
| chr10:61429660 | C | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.385-514G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429660 | |||||||
| chr10:61429818 | A | G | 1 | a0001c0002t0005g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-672T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429818 | |||||||
| chr10:61429885 | G | A | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.385-739C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429885 | |||||||
| chr10:61429929 | A | G | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.385-783T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61429929 | |||||||
| chr10:61430053 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.385-907A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430053 | |||||||
| chr10:61430061 | G | A | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.385-915C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430061 | |||||||
| chr10:61430128 | TTA | T | 12 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(9): Show |
15 | HG00597.hp1 HG00609.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-984_385-983del others(2): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430128 | |||||||
| chr10:61430164 | T | C | 13 | a0001c0001t0001g0206 a0001c0001t0002g0003 a0001c0001t0002g0035 others(10): Show |
21 | HG00438.hp2 HG00639.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.385-1018A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430164 | |||||||
| chr10:61430188 | C | A | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+1031G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430188 | |||||||
| chr10:61430254 | T | C | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+965A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430254 | |||||||
| chr10:61430380 | G | T | 1 | a0001c0002t0017g0264 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.384+839C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430380 | |||||||
| chr10:61430402 | T | G | 1 | a0001c0001t0001g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.384+817A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430402 | |||||||
| chr10:61430428 | C | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0075 a0001c0001t0001g0095 others(3): Show |
7 | HG00323.hp2 HG01168.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+791G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430428 | |||||||
| chr10:61430469 | G | A | 11 | a0001c0002t0005g0041 a0001c0002t0005g0043 a0001c0002t0005g0044 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.384+750C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430469 | |||||||
| chr10:61430520 | C | T | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+699G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430520 | |||||||
| chr10:61430535 | ACATAATT | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+677_384+683del others(7): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430535 | |||||||
| chr10:61430543 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+676C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430543 | |||||||
| chr10:61430550 | T | C | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.384+669A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430550 | |||||||
| chr10:61430571 | C | CAA | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+646_384+647dup others(2): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430571 | |||||||
| chr10:61430571 | CA | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0149 a0001c0001t0002g0151 others(31): Show |
44 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.384+647delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430571 | |||||||
| chr10:61430762 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.384+457C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61430762 | |||||||
| chr10:61431072 | A | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+147T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61431072 | |||||||
| chr10:61431080 | T | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0033g0116 |
3 | HG01081.hp2 HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.384+139A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61431080 | |||||||
| chr10:61431091 | C | G | 50 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0002 others(47): Show |
71 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.384+128G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 3/5 | chr10 | 61431091 | |||||||
| chr10:61431416 | A | G | 2 | a0001c0002t0004g0248 a0001c0002t0004g0256 |
2 | NA18612.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.271-84T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431416 | |||||||
| chr10:61431527 | C | T | 45 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0002 others(42): Show |
66 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.271-195G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431527 | |||||||
| chr10:61431551 | A | G | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-219T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431551 | |||||||
| chr10:61431715 | G | GT | 14 | a0001c0001t0001g0083 a0001c0001t0001g0168 a0001c0001t0002g0031 others(11): Show |
17 | HG00597.hp1 HG00609.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-384dupA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431715 | |||||||
| chr10:61431715 | GT | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
13 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-384delA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431715 | |||||||
| chr10:61431857 | A | C | 5 | a0001c0001t0043g0270 a0001c0002t0005g0267 a0001c0002t0005g0268 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-525T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431857 | |||||||
| chr10:61431886 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-554G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431886 | |||||||
| chr10:61431887 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-555A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431887 | |||||||
| chr10:61431888 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-556G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431888 | |||||||
| chr10:61431964 | T | C | 2 | a0001c0002t0005g0041 a0001c0002t0005g0043 |
4 | HG01109.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-632A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61431964 | |||||||
| chr10:61432394 | G | A | 2 | a0001c0002t0009g0161 a0004c0005t0003g0158 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.271-1062C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432394 | |||||||
| chr10:61432440 | A | G | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1108T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432440 | |||||||
| chr10:61432626 | A | G | 1 | a0001c0002t0004g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271-1294T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432626 | |||||||
| chr10:61432649 | AT | A | 87 | a0001c0001t0001g0082 a0001c0001t0001g0168 a0001c0001t0001g0185 others(84): Show |
118 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-1318delA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432649 | |||||||
| chr10:61432656 | T | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(142): Show |
190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.271-1324A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432656 | |||||||
| chr10:61432656 | TA | T | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-1325delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432656 | |||||||
| chr10:61432887 | G | A | 3 | a0001c0001t0003g0177 a0001c0001t0003g0180 a0001c0001t0003g0181 |
3 | HG00639.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.271-1555C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61432887 | |||||||
| chr10:61433040 | A | G | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1708T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433040 | |||||||
| chr10:61433088 | C | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.271-1756G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433088 | |||||||
| chr10:61433133 | T | A | 12 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(9): Show |
15 | HG00597.hp1 HG00609.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-1801A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433133 | |||||||
| chr10:61433185 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1853C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433185 | |||||||
| chr10:61433293 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.271-1961T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433293 | |||||||
| chr10:61433420 | A | T | 7 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0009g0161 others(4): Show |
8 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-2088T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433420 | |||||||
| chr10:61433594 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.271-2262T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433594 | |||||||
| chr10:61433637 | T | A | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-2305A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433637 | |||||||
| chr10:61433723 | C | T | 155 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(152): Show |
202 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.271-2391G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433723 | |||||||
| chr10:61433812 | A | G | 1 | a0001c0001t0023g0222 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.270+2358T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433812 | |||||||
| chr10:61433839 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0056 |
3 | HG00597.hp2 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.270+2331A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433839 | |||||||
| chr10:61433956 | T | C | 1 | a0001c0001t0006g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.270+2214A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433956 | |||||||
| chr10:61433977 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.270+2193C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61433977 | |||||||
| chr10:61434276 | G | A | 3 | a0001c0002t0012g0159 a0001c0002t0012g0163 a0001c0002t0012g0164 |
3 | HG00738.hp1 HG02293.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.270+1894C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434276 | |||||||
| chr10:61434366 | C | T | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
91 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.270+1804G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434366 | |||||||
| chr10:61434367 | G | T | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+1803C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434367 | |||||||
| chr10:61434418 | G | T | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+1752C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434418 | |||||||
| chr10:61434818 | G | A | 27 | a0001c0002t0004g0006 a0001c0002t0004g0014 a0001c0002t0004g0015 others(24): Show |
35 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+1352C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434818 | |||||||
| chr10:61434971 | T | C | 2 | a0001c0001t0034g0152 a0001c0001t0036g0153 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.270+1199A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61434971 | |||||||
| chr10:61435016 | G | A | 2 | a0001c0002t0009g0030 a0001c0002t0009g0160 |
3 | HG02055.hp1 HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.270+1154C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435016 | |||||||
| chr10:61435041 | T | C | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.270+1129A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435041 | |||||||
| chr10:61435084 | A | C | 1 | a0001c0001t0002g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.270+1086T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435084 | |||||||
| chr10:61435095 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.270+1075C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435095 | |||||||
| chr10:61435102 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.270+1068T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435102 | |||||||
| chr10:61435273 | C | T | 9 | a0001c0001t0006g0021 a0001c0001t0006g0039 a0001c0001t0006g0225 others(6): Show |
11 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+897G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435273 | |||||||
| chr10:61435383 | G | A | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+787C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435383 | |||||||
| chr10:61435411 | C | T | 7 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0195 others(4): Show |
7 | NA18942.hp2 NA18961.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+759G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435411 | |||||||
| chr10:61435557 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.270+613T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435557 | |||||||
| chr10:61435803 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.270+367G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435803 | |||||||
| chr10:61435996 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0219 |
3 | HG02559.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.270+174A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61435996 | |||||||
| chr10:61436101 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+69T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61436101 | |||||||
| chr10:61436151 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.270+19T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 2/5 | chr10 | 61436151 | |||||||
| chr10:61436299 | C | CA | 5 | a0001c0001t0003g0011 a0001c0001t0003g0181 a0001c0001t0003g0184 others(2): Show |
8 | HG02258.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-52dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436299 | |||||||
| chr10:61436371 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.192-123C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436371 | |||||||
| chr10:61436376 | A | C | 145 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(142): Show |
191 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.192-128T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436376 | |||||||
| chr10:61436453 | C | T | 1 | a0001c0002t0011g0066 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.192-205G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436453 | |||||||
| chr10:61436846 | A | G | 2 | a0001c0001t0023g0222 a0001c0001t0028g0224 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.192-598T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436846 | |||||||
| chr10:61436863 | T | C | 14 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(11): Show |
17 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.192-615A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436863 | |||||||
| chr10:61436882 | C | T | 3 | a0001c0001t0020g0134 a0001c0001t0029g0067 a0001c0002t0011g0066 |
3 | HG02895.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192-634G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61436882 | |||||||
| chr10:61437127 | C | T | 45 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0002 others(42): Show |
66 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.192-879G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437127 | |||||||
| chr10:61437204 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.192-956A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437204 | |||||||
| chr10:61437238 | A | G | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-990T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437238 | |||||||
| chr10:61437303 | G | A | 1 | a0001c0002t0011g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-1055C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437303 | |||||||
| chr10:61437354 | C | G | 1 | a0001c0001t0035g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.192-1106G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437354 | |||||||
| chr10:61437470 | A | G | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.192-1222T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437470 | |||||||
| chr10:61437602 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.192-1354C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437602 | |||||||
| chr10:61437646 | A | G | 1 | a0001c0001t0036g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192-1398T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437646 | |||||||
| chr10:61437778 | C | T | 17 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
20 | HG01167.hp1 HG01192.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.192-1530G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437778 | |||||||
| chr10:61437797 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-1549G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437797 | |||||||
| chr10:61437844 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-1596G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437844 | |||||||
| chr10:61437901 | C | T | 45 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0002 others(42): Show |
66 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.192-1653G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437901 | |||||||
| chr10:61437902 | G | A | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.192-1654C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437902 | |||||||
| chr10:61437950 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-1702T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61437950 | |||||||
| chr10:61438114 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192-1866G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61438114 | |||||||
| chr10:61438139 | A | T | 1 | a0001c0001t0006g0039 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.192-1891T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61438139 | |||||||
| chr10:61438429 | G | C | 2 | a0001c0001t0034g0152 a0001c0001t0036g0153 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.192-2181C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61438429 | |||||||
| chr10:61438799 | C | T | 1 | a0001c0001t0006g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.192-2551G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61438799 | |||||||
| chr10:61439017 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.192-2769C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439017 | |||||||
| chr10:61439070 | G | C | 4 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0218 others(1): Show |
4 | HG00673.hp1 NA18980.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-2822C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439070 | |||||||
| chr10:61439075 | G | A | 1 | a0001c0002t0016g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.192-2827C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439075 | |||||||
| chr10:61439085 | A | G | 1 | a0001c0002t0016g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.192-2837T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439085 | |||||||
| chr10:61439336 | C | G | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-3088G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439336 | |||||||
| chr10:61439421 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG00642.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-3173G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439421 | |||||||
| chr10:61439494 | A | T | 1 | a0001c0001t0002g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.192-3246T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439494 | |||||||
| chr10:61439761 | T | C | 21 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(18): Show |
28 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.192-3513A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439761 | |||||||
| chr10:61439921 | T | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-3673A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439921 | |||||||
| chr10:61439961 | C | T | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-3713G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61439961 | |||||||
| chr10:61440040 | G | A | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
16 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.192-3792C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440040 | |||||||
| chr10:61440066 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0030g0081 |
2 | NA18942.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.192-3818G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440066 | |||||||
| chr10:61440076 | C | T | 12 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0073 others(9): Show |
14 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.192-3828G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440076 | |||||||
| chr10:61440177 | T | C | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-3929A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440177 | |||||||
| chr10:61440310 | G | A | 1 | a0001c0001t0008g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.192-4062C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440310 | |||||||
| chr10:61440444 | C | T | 1 | a0001c0002t0004g0258 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.192-4196G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440444 | |||||||
| chr10:61440487 | A | G | 4 | a0001c0001t0043g0270 a0001c0002t0005g0267 a0001c0002t0005g0268 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-4239T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440487 | |||||||
| chr10:61440514 | C | CA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(95): Show |
132 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.192-4267dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440514 | |||||||
| chr10:61440514 | CA | C | 81 | a0001c0001t0001g0038 a0001c0001t0001g0168 a0001c0001t0001g0203 others(78): Show |
115 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.192-4267delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440514 | |||||||
| chr10:61440539 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-4291C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440539 | |||||||
| chr10:61440747 | G | A | 17 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
20 | HG01167.hp1 HG01192.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.192-4499C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440747 | |||||||
| chr10:61440759 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-4511C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440759 | |||||||
| chr10:61440833 | C | A | 1 | a0001c0002t0016g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.192-4585G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440833 | |||||||
| chr10:61440881 | C | T | 1 | a0001c0001t0039g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192-4633G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440881 | |||||||
| chr10:61440937 | C | T | 1 | a0001c0001t0025g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.192-4689G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61440937 | |||||||
| chr10:61441006 | G | T | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-4758C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441006 | |||||||
| chr10:61441108 | C | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.192-4860G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441108 | |||||||
| chr10:61441205 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.192-4957G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441205 | |||||||
| chr10:61441206 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.192-4958C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441206 | |||||||
| chr10:61441250 | G | T | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.192-5002C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441250 | |||||||
| chr10:61441305 | T | A | 1 | a0006c0006t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192-5057A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441305 | |||||||
| chr10:61441487 | G | A | 1 | a0001c0002t0004g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.192-5239C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441487 | |||||||
| chr10:61441613 | T | A | 1 | a0001c0002t0009g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192-5365A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441613 | |||||||
| chr10:61441688 | G | C | 1 | a0001c0002t0005g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.192-5440C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441688 | |||||||
| chr10:61441689 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-5441T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441689 | |||||||
| chr10:61441794 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.192-5546T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441794 | |||||||
| chr10:61441953 | C | G | 10 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0009g0161 others(7): Show |
11 | HG00738.hp1 HG02055.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-5705G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61441953 | |||||||
| chr10:61442013 | C | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-5765G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442013 | |||||||
| chr10:61442042 | TTTTA | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-5798_192-5795d others(6): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442042 | |||||||
| chr10:61442063 | G | GTA | 25 | a0001c0001t0001g0127 a0001c0001t0003g0005 a0001c0001t0003g0011 others(22): Show |
32 | HG00609.hp1 HG00639.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.192-5817_192-5816d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442063 | |||||||
| chr10:61442063 | G | GTATA | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-5819_192-5816d others(6): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442063 | |||||||
| chr10:61442095 | C | G | 3 | a0001c0001t0003g0130 a0001c0001t0003g0146 a0001c0001t0003g0147 |
3 | NA18956.hp1 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.192-5847G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442095 | |||||||
| chr10:61442101 | T | G | 3 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0234 |
3 | HG00609.hp1 NA19076.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.192-5853A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442101 | |||||||
| chr10:61442284 | C | G | 10 | a0001c0002t0009g0030 a0001c0002t0009g0160 a0001c0002t0009g0161 others(7): Show |
11 | HG00738.hp1 HG02055.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-6036G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442284 | |||||||
| chr10:61442311 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.192-6063A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442311 | |||||||
| chr10:61442485 | T | C | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.192-6237A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442485 | |||||||
| chr10:61442653 | G | A | 20 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
23 | HG01167.hp1 HG01192.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.192-6405C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442653 | |||||||
| chr10:61442761 | T | C | 3 | a0001c0001t0003g0130 a0001c0001t0003g0146 a0001c0001t0003g0147 |
3 | NA18956.hp1 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.192-6513A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61442761 | |||||||
| chr10:61443199 | T | C | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.192-6951A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443199 | |||||||
| chr10:61443296 | C | CA | 23 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0104 others(20): Show |
25 | HG00323.hp1 HG01243.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.192-7049dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443296 | |||||||
| chr10:61443296 | CA | C | 34 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0110 others(31): Show |
44 | HG00597.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.192-7049delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443296 | |||||||
| chr10:61443333 | C | T | 1 | a0001c0002t0005g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192-7085G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443333 | |||||||
| chr10:61443357 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.192-7109G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443357 | |||||||
| chr10:61443358 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-7110C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443358 | |||||||
| chr10:61443441 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-7193C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443441 | |||||||
| chr10:61443464 | C | CA | 30 | a0001c0001t0001g0108 a0001c0001t0001g0168 a0001c0001t0002g0031 others(27): Show |
40 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.192-7217dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443464 | |||||||
| chr10:61443583 | C | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-7335G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443583 | |||||||
| chr10:61443691 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.192-7443G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443691 | |||||||
| chr10:61443770 | T | C | 1 | a0004c0005t0003g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.192-7522A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443770 | |||||||
| chr10:61443804 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.192-7556G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443804 | |||||||
| chr10:61443881 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0023g0222 a0001c0001t0028g0224 |
3 | HG02451.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.192-7633C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61443881 | |||||||
| chr10:61444170 | T | A | 1 | a0001c0001t0002g0210 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.192-7922A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444170 | |||||||
| chr10:61444315 | C | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-8067G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444315 | |||||||
| chr10:61444596 | A | C | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.191+8295T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444596 | |||||||
| chr10:61444608 | C | T | 11 | a0001c0002t0005g0041 a0001c0002t0005g0043 a0001c0002t0005g0044 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+8283G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444608 | |||||||
| chr10:61444645 | T | A | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+8246A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444645 | |||||||
| chr10:61444653 | T | TA | 28 | a0001c0001t0001g0057 a0001c0001t0001g0093 a0001c0001t0001g0109 others(25): Show |
31 | HG00609.hp1 HG01952.hp2 HG02273.hp1 others(28): Show |
intron_variant | MODIFIER | c.191+8237dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444653 | |||||||
| chr10:61444653 | T | TAA | 58 | a0001c0001t0001g0038 a0001c0001t0001g0203 a0001c0001t0001g0206 others(55): Show |
81 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.191+8236_191+8237d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444653 | |||||||
| chr10:61444653 | TA | T | 24 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0137 others(21): Show |
31 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+8237delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444653 | |||||||
| chr10:61444653 | TAA | T | 7 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(4): Show |
9 | HG00597.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+8236_191+8237d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444653 | |||||||
| chr10:61444664 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.191+8227T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444664 | |||||||
| chr10:61444904 | G | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+7987C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444904 | |||||||
| chr10:61444935 | C | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+7956G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61444935 | |||||||
| chr10:61445048 | C | T | 7 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(4): Show |
7 | HG00609.hp1 HG02717.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+7843G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445048 | |||||||
| chr10:61445185 | T | A | 1 | a0001c0002t0004g0256 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.191+7706A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445185 | |||||||
| chr10:61445242 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.191+7649G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445242 | |||||||
| chr10:61445592 | T | C | 1 | a0001c0002t0013g0245 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.191+7299A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445592 | |||||||
| chr10:61445676 | A | T | 1 | a0001c0001t0002g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.191+7215T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445676 | |||||||
| chr10:61445677 | T | C | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+7214A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445677 | |||||||
| chr10:61445684 | TTA | T | 20 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
27 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+7205_191+7206d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445684 | |||||||
| chr10:61445686 | A | T | 5 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(2): Show |
5 | HG00609.hp1 HG02056.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+7205T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445686 | |||||||
| chr10:61445700 | A | G | 6 | a0001c0001t0043g0270 a0001c0002t0005g0267 a0001c0002t0005g0268 others(3): Show |
6 | HG02630.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+7191T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445700 | |||||||
| chr10:61445715 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.191+7176T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445715 | |||||||
| chr10:61445850 | C | G | 158 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(155): Show |
206 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.191+7041G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61445850 | |||||||
| chr10:61446007 | G | GA | 47 | a0001c0001t0001g0057 a0001c0001t0043g0270 a0001c0002t0004g0006 others(44): Show |
59 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.191+6883dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446007 | |||||||
| chr10:61446033 | T | C | 80 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(77): Show |
106 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.191+6858A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446033 | |||||||
| chr10:61446126 | C | A | 1 | a0001c0002t0011g0066 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.191+6765G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446126 | |||||||
| chr10:61446279 | A | G | 1 | a0001c0001t0019g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.191+6612T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446279 | |||||||
| chr10:61446389 | C | A | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.191+6502G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446389 | |||||||
| chr10:61446403 | C | G | 79 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(76): Show |
105 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.191+6488G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446403 | |||||||
| chr10:61446603 | G | A | 100 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(97): Show |
133 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.191+6288C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446603 | |||||||
| chr10:61446732 | T | C | 2 | a0001c0001t0003g0187 a0001c0001t0018g0046 |
2 | HG01070.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.191+6159A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446732 | |||||||
| chr10:61446736 | T | C | 1 | a0001c0002t0004g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.191+6155A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446736 | |||||||
| chr10:61446817 | C | CA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0052 others(10): Show |
16 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.191+6073dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAA | 6 | a0001c0001t0002g0223 a0001c0001t0006g0039 a0001c0001t0006g0227 others(3): Show |
7 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+6072_191+6073d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0007g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.191+6063_191+6073d others(13): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0151 a0001c0001t0007g0234 |
2 | NA19081.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.191+6062_191+6073d others(14): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0036g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+6060_191+6073d others(16): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0034g0152 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191+6059_191+6073d others(17): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0035g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.191+6055_191+6073d others(21): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CA | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(43): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.191+6073delT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAA | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(30): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.191+6072_191+6073d others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAA | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0189 others(5): Show |
8 | HG00673.hp1 HG02922.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.191+6071_191+6073d others(5): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAA | C | 21 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0150 others(18): Show |
27 | HG00733.hp2 HG01106.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.191+6070_191+6073d others(6): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAA | C | 45 | a0001c0001t0001g0148 a0001c0001t0001g0203 a0001c0001t0001g0206 others(42): Show |
68 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.191+6069_191+6073d others(7): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAAA | C | 35 | a0001c0001t0002g0012 a0001c0001t0002g0188 a0001c0001t0002g0191 others(32): Show |
46 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.191+6068_191+6073d others(8): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAAAA | C | 10 | a0001c0001t0007g0232 a0001c0001t0025g0142 a0001c0002t0004g0236 others(7): Show |
10 | HG00609.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+6067_191+6073d others(9): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0043g0270 a0001c0002t0005g0041 a0001c0002t0005g0043 others(10): Show |
17 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.191+6066_191+6073d others(10): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0007g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.191+6063_191+6073d others(13): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446817 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0190 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.191+6062_191+6073d others(14): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446817 | |||||||
| chr10:61446883 | GACACAGA others(1): Show |
G | 166 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(163): Show |
216 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.191+6000_191+6007d others(10): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446883 | |||||||
| chr10:61446969 | T | TA | 58 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(55): Show |
73 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.191+5921dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61446969 | |||||||
| chr10:61447064 | C | A | 5 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(2): Show |
5 | HG00609.hp1 HG03688.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+5827G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447064 | |||||||
| chr10:61447164 | C | CATACAAA others(24): Show |
1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.191+5726_191+5727i others(33): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447164 | |||||||
| chr10:61447174 | T | C | 1 | a0001c0001t0036g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+5717A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447174 | |||||||
| chr10:61447191 | G | T | 3 | a0001c0001t0020g0134 a0001c0001t0029g0067 a0001c0002t0011g0066 |
3 | HG02895.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191+5700C>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447191 | |||||||
| chr10:61447391 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.191+5500A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447391 | |||||||
| chr10:61447433 | G | C | 3 | a0001c0001t0002g0223 a0001c0001t0023g0222 a0001c0001t0028g0224 |
3 | HG02451.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.191+5458C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447433 | |||||||
| chr10:61447522 | G | C | 1 | a0001c0002t0012g0164 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.191+5369C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447522 | |||||||
| chr10:61447626 | G | A | 2 | a0001c0002t0011g0165 a0001c0002t0011g0166 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.191+5265C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61447626 | |||||||
| chr10:61448078 | C | T | 12 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
15 | HG01952.hp2 HG02273.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+4813G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448078 | |||||||
| chr10:61448079 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.191+4812C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448079 | |||||||
| chr10:61448126 | G | A | 2 | a0001c0001t0006g0039 a0002c0003t0006g0048 |
3 | HG01257.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.191+4765C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448126 | |||||||
| chr10:61448207 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0219 |
3 | HG02559.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.191+4684C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448207 | |||||||
| chr10:61448252 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.191+4639G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448252 | |||||||
| chr10:61448424 | C | T | 1 | a0001c0001t0025g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.191+4467G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448424 | |||||||
| chr10:61448503 | A | G | 1 | a0001c0002t0004g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191+4388T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448503 | |||||||
| chr10:61448523 | C | T | 47 | a0001c0001t0001g0038 a0001c0001t0001g0203 a0001c0001t0001g0206 others(44): Show |
69 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.191+4368G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448523 | |||||||
| chr10:61448577 | C | T | 1 | a0001c0002t0004g0042 | 2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.191+4314G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448577 | |||||||
| chr10:61448619 | GT | G | 83 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(80): Show |
111 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.191+4271delA | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448619 | |||||||
| chr10:61448883 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.191+4008A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448883 | |||||||
| chr10:61448910 | A | G | 1 | a0001c0002t0016g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.191+3981T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448910 | |||||||
| chr10:61448950 | A | G | 1 | a0001c0001t0025g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.191+3941T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61448950 | |||||||
| chr10:61449045 | T | C | 1 | a0001c0002t0017g0264 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.191+3846A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449045 | |||||||
| chr10:61449084 | C | G | 1 | a0001c0001t0003g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.191+3807G>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449084 | |||||||
| chr10:61449149 | T | C | 2 | a0001c0002t0016g0235 a0001c0002t0016g0265 |
2 | HG01433.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.191+3742A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449149 | |||||||
| chr10:61449197 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.191+3694G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449197 | |||||||
| chr10:61449373 | G | A | 25 | a0001c0001t0001g0185 a0001c0001t0003g0005 a0001c0001t0003g0011 others(22): Show |
32 | HG00609.hp1 HG00639.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.191+3518C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449373 | |||||||
| chr10:61449876 | T | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0001g0133 |
4 | HG00544.hp2 NA18971.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+3015A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449876 | |||||||
| chr10:61449926 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.191+2965A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449926 | |||||||
| chr10:61449944 | T | G | 1 | a0001c0001t0002g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.191+2947A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449944 | |||||||
| chr10:61449998 | C | A | 1 | a0001c0001t0020g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.191+2893G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61449998 | |||||||
| chr10:61450048 | T | C | 2 | a0001c0001t0034g0152 a0001c0001t0036g0153 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+2843A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450048 | |||||||
| chr10:61450181 | G | GA | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.191+2709dupT | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450181 | |||||||
| chr10:61450205 | A | T | 1 | a0001c0002t0005g0041 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.191+2686T>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450205 | |||||||
| chr10:61450276 | A | C | 1 | a0001c0001t0003g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.191+2615T>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450276 | |||||||
| chr10:61450297 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.191+2594C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450297 | |||||||
| chr10:61450363 | C | T | 1 | a0001c0002t0016g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.191+2528G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450363 | |||||||
| chr10:61450585 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.191+2306A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450585 | |||||||
| chr10:61450619 | A | G | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+2272T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450619 | |||||||
| chr10:61450650 | T | TTTCTTTG others(354): Show |
1 | a0001c0001t0018g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.191+2240_191+2241i others(363): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450650 | |||||||
| chr10:61450650 | T | TTTCTTTG others(355): Show |
1 | a0001c0001t0003g0187 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191+2240_191+2241i others(364): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450650 | |||||||
| chr10:61450763 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0002g0031 a0001c0001t0002g0167 others(5): Show |
11 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.191+2128C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450763 | |||||||
| chr10:61450798 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.191+2093T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450798 | |||||||
| chr10:61450806 | T | C | 1 | a0001c0002t0005g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.191+2085A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450806 | |||||||
| chr10:61450843 | G | C | 21 | a0001c0001t0001g0185 a0001c0001t0003g0005 a0001c0001t0003g0011 others(18): Show |
28 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.191+2048C>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450843 | |||||||
| chr10:61450862 | T | G | 46 | a0001c0001t0001g0038 a0001c0001t0001g0203 a0001c0001t0001g0206 others(43): Show |
68 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.191+2029A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450862 | |||||||
| chr10:61450967 | A | G | 3 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
3 | NA18950.hp2 NA18990.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.191+1924T>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61450967 | |||||||
| chr10:61451050 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.191+1841G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451050 | |||||||
| chr10:61451136 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG00642.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+1755A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451136 | |||||||
| chr10:61451304 | C | A | 1 | a0001c0001t0003g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.191+1587G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451304 | |||||||
| chr10:61451379 | C | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+1512G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451379 | |||||||
| chr10:61451584 | T | C | 6 | a0001c0001t0043g0270 a0001c0002t0005g0267 a0001c0002t0005g0268 others(3): Show |
6 | HG02630.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+1307A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451584 | |||||||
| chr10:61451678 | G | A | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+1213C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451678 | |||||||
| chr10:61451911 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+980G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451911 | |||||||
| chr10:61451959 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.191+932G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451959 | |||||||
| chr10:61451986 | G | GAT | 20 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
27 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.191+903_191+904dup others(2): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451986 | |||||||
| chr10:61451986 | GAT | G | 21 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(18): Show |
24 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.191+903_191+904del others(2): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451986 | |||||||
| chr10:61451986 | GATAT | G | 140 | a0001c0001t0001g0038 a0001c0001t0001g0168 a0001c0001t0001g0185 others(137): Show |
186 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.191+901_191+904del others(4): Show |
TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451986 | |||||||
| chr10:61451988 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.191+903A>C | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61451988 | |||||||
| chr10:61452119 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.191+772C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452119 | |||||||
| chr10:61452193 | G | A | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+698C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452193 | |||||||
| chr10:61452339 | T | C | 164 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 others(161): Show |
213 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.191+552A>G | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452339 | |||||||
| chr10:61452359 | C | T | 1 | a0001c0001t0035g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.191+532G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452359 | |||||||
| chr10:61452369 | G | A | 1 | a0001c0001t0039g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.191+522C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452369 | |||||||
| chr10:61452515 | C | T | 46 | a0001c0001t0043g0270 a0001c0002t0004g0006 a0001c0002t0004g0014 others(43): Show |
58 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+376G>A | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452515 | |||||||
| chr10:61452524 | C | A | 3 | a0001c0001t0002g0223 a0001c0001t0023g0222 a0001c0001t0028g0224 |
3 | HG02451.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.191+367G>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452524 | |||||||
| chr10:61452609 | G | A | 8 | a0001c0001t0006g0039 a0001c0001t0006g0225 a0001c0001t0006g0226 others(5): Show |
9 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+282C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452609 | |||||||
| chr10:61452627 | T | A | 1 | a0001c0001t0008g0040 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+264A>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452627 | |||||||
| chr10:61452814 | G | A | 4 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(1): Show |
4 | HG00609.hp1 HG03688.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+77C>T | TMEM26 | ENSG00000196932.12 | transcript | ENST00000399298.8 | protein_coding | 1/5 | chr10 | 61452814 |