Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 339855 |
| ensemblid | ENSG00000174611.12 |
| hgncid | 26576 |
| symbol | KY |
| name | kyphoscoliosis peptidase |
| refseq_nuc | NM_178554.6 |
| refseq_prot | NP_848649.3 |
| ensembl_nuc | ENST00000423778.7 |
| ensembl_prot | ENSP00000397598.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 134599923 |
| end | 134651022 |
| strand | - |
| ver | v1.2 |
| region | chr3:134599923-134651022 |
| region5000 | chr3:134594923-134656022 |
| regionname0 | KY_chr3_134599923_134651022 |
| regionname5000 | KY_chr3_134594923_134656022 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 661 | 288 | 84 | 60 | 84 | 14 | 44 | 70 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| a0002 | 0/0 | 661 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| a0003 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| a0004 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| a0005 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| a0006 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | MELKK others(656): Show |
chr3 | 134594923 | 134656022 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1983 | 145 | 27 | 36 | 49 | 10 | 22 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0002 | 0/0 | 1983 | 61 | 21 | 8 | 18 | 1 | 13 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0003 | 0/0 | 1983 | 29 | 7 | 7 | 7 | 2 | 6 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0004 | 0/0 | 1983 | 18 | 16 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0005 | 0/0 | 1983 | 14 | 6 | 1 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0006 | 0/0 | 1983 | 12 | 3 | 5 | 0 | 1 | 3 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0007 | 0/0 | 1983 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0008 | 0/0 | 1983 | 3 | 0 | 0 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0009 | 1/0 | 1983 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0001c0012 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0002c0010 | 0/0 | 1983 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0003c0013 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0004c0014 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0005c0015 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 | ||
| a0006c0011 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATGGA others(1978): Show |
chr3 | 134594923 | 134656022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5714 | 111 | 22 | 27 | 42 | 7 | 12 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0003 | 0/0 | 5714 | 9 | 0 | 1 | 0 | 3 | 5 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0005 | 0/0 | 5714 | 10 | 0 | 5 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0008 | 0/0 | 5714 | 4 | 4 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0012 | 0/0 | 5714 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0013 | 0/0 | 5714 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0014 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0022 | 0/0 | 5714 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0023 | 0/0 | 5714 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0024 | 0/0 | 5714 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0025 | 0/0 | 5714 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0027 | 0/0 | 5714 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0001t0029 | 0/0 | 5714 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0002 | 0/0 | 5715 | 42 | 17 | 7 | 5 | 1 | 12 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0004 | 0/0 | 5715 | 13 | 2 | 0 | 11 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0015 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0018 | 0/0 | 5714 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0019 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0020 | 0/0 | 5704 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5699): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0021 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0002t0030 | 0/0 | 5715 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0003t0002 | 0/0 | 5715 | 29 | 7 | 7 | 7 | 2 | 6 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0004t0001 | 0/0 | 5714 | 15 | 13 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0004t0011 | 0/0 | 5714 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0005t0006 | 0/0 | 5715 | 8 | 1 | 0 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0005t0007 | 0/0 | 5715 | 5 | 4 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0005t0016 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0006t0001 | 0/0 | 5714 | 5 | 3 | 1 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0006t0003 | 0/0 | 5714 | 6 | 0 | 4 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0006t0026 | 0/0 | 5714 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0007t0010 | 0/0 | 5715 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0001c0008t0001 | 0/0 | 5714 | 3 | 0 | 0 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0001c0009t0009 | 1/0 | 5704 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5699): Show |
chr3 | 134594923 | 134656022 |
| a0001c0012t0028 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5709): Show |
chr3 | 134594923 | 134656022 |
| a0002c0010t0002 | 0/0 | 5715 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0003c0013t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0004c0014t0017 | 0/0 | 5704 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5699): Show |
chr3 | 134594923 | 134656022 |
| a0005c0015t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5710): Show |
chr3 | 134594923 | 134656022 |
| a0006c0011t0009 | 0/0 | 5704 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | ATTTG others(5699): Show |
chr3 | 134594923 | 134656022 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 4 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0003 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0013g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0022g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0023g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0024g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0025g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0027g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0001t0029g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0018g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0019g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0002t0030g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0004t0011g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0005t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0006t0026g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0007t0010g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0007t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0008t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0008t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0009t0009g0014 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0001c0012t0028g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0002c0010t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0002c0010t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0003c0013t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0004c0014t0017g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0005c0015t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| a0006c0011t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0120 | EUR | GBR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0065 | EUR | FIN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | FIN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00621 | hp2 | a0003 | c0013 | t0002 | g0115 | EAS | CHS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00642 | hp1 | a0001 | c0006 | t0003 | g0236 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0208 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG00741 | hp2 | a0001 | c0006 | t0003 | g0234 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0217 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01081 | hp2 | a0001 | c0001 | t0023 | g0191 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0230 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01109 | hp1 | a0001 | c0005 | t0007 | g0033 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01255 | hp2 | a0001 | c0002 | t0030 | g0239 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0229 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01256 | hp2 | a0001 | c0006 | t0003 | g0028 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01258 | hp2 | a0001 | c0006 | t0003 | g0028 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0218 | EUR | IBS | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01884 | hp1 | a0004 | c0014 | t0017 | g0081 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01891 | hp1 | a0001 | c0004 | t0011 | g0008 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01952 | hp2 | a0001 | c0001 | t0012 | g0171 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0206 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02004 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02055 | hp1 | a0001 | c0007 | t0010 | g0083 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02056 | hp2 | a0001 | c0008 | t0001 | g0185 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02074 | hp1 | a0005 | c0015 | t0002 | g0238 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0210 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PEL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02451 | hp1 | a0001 | c0002 | t0019 | g0098 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02572 | hp2 | a0001 | c0005 | t0007 | g0048 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0209 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02622 | hp2 | a0001 | c0002 | t0021 | g0060 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0214 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02683 | hp1 | a0001 | c0006 | t0026 | g0207 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02698 | hp2 | a0001 | c0001 | t0029 | g0195 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0166 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0189 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0216 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02738 | hp1 | a0001 | c0006 | t0003 | g0235 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0225 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02818 | hp1 | a0001 | c0005 | t0016 | g0153 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02896 | hp1 | a0001 | c0012 | t0028 | g0203 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0220 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0042 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02970 | hp2 | a0001 | c0004 | t0011 | g0008 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0045 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03139 | hp1 | a0001 | c0005 | t0007 | g0082 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03209 | hp1 | a0001 | c0007 | t0010 | g0015 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0173 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0011 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03453 | hp1 | a0001 | c0009 | t0009 | g0014 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03453 | hp2 | a0001 | c0004 | t0011 | g0008 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0174 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03579 | hp2 | a0001 | c0005 | t0007 | g0046 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0224 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03669 | hp1 | a0001 | c0006 | t0003 | g0237 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0228 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0118 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0227 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0117 | SAS | PJL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03831 | hp2 | a0001 | c0001 | t0027 | g0148 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03834 | hp2 | a0001 | c0002 | t0018 | g0106 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04184 | hp2 | a0001 | c0001 | t0025 | g0170 | SAS | BEB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04204 | hp1 | a0001 | c0001 | t0013 | g0190 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0119 | SAS | STU | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18906 | hp2 | a0001 | c0005 | t0007 | g0047 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18939 | hp2 | a0002 | c0010 | t0002 | g0212 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18941 | hp1 | a0001 | c0002 | t0020 | g0039 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18951 | hp1 | a0001 | c0005 | t0006 | g0105 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18956 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18956 | hp2 | a0001 | c0008 | t0001 | g0025 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18960 | hp2 | a0001 | c0005 | t0006 | g0160 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18967 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18967 | hp2 | a0001 | c0005 | t0006 | g0199 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18968 | hp1 | a0001 | c0002 | t0015 | g0088 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18969 | hp1 | a0001 | c0005 | t0006 | g0158 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18982 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18984 | hp2 | a0001 | c0005 | t0006 | g0104 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0233 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18999 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19010 | hp2 | a0001 | c0008 | t0001 | g0025 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19030 | hp2 | a0006 | c0011 | t0009 | g0031 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19057 | hp1 | a0001 | c0005 | t0006 | g0200 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19068 | hp1 | a0002 | c0010 | t0002 | g0213 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19076 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19077 | hp1 | a0001 | c0001 | t0024 | g0196 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19082 | hp1 | a0001 | c0001 | t0022 | g0136 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19090 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19091 | hp2 | a0001 | c0005 | t0006 | g0159 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0011 | AFR | YRI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0011 | AFR | ASW | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | ASW | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0007 | EUR | TSI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0007 | EUR | TSI | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | GIH | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | GIH | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG01123 | hp2 | a0001 | c0007 | t0010 | g0015 | AMR | CLM | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | USA | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | USA | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | USA | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | USA | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| homoSapiens_grch38 | hp1 | a0001 | c0009 | t0009 | g0014 | REF | REF | KY_chr3_134594923_134656022 | KY | chr3 | 134594923 | 134656022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134603788 | G | A | 1 | a0003 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1777C>T | p.Arg593Trp | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1839/5704 | 1777/1986 | 593/661 | chr3 | 134603788 | |||
| chr3:134603805 | C | G | 1 | a0005 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1760G>C | p.Gly587Ala | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1822/5704 | 1760/1986 | 587/661 | chr3 | 134603805 | |||
| chr3:134610219 | G | C | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.875C>G | p.Thr292Ser | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/11 | 937/5704 | 875/1986 | 292/661 | chr3 | 134610219 | |||
| chr3:134610363 | A | G | 1 | a0002 | 2 | NA18939.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.731T>C | p.Met244Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/11 | 793/5704 | 731/1986 | 244/661 | chr3 | 134610363 | |||
| chr3:134620833 | C | T | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.508G>A | p.Glu170Lys | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/11 | 570/5704 | 508/1986 | 170/661 | chr3 | 134620833 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134603672 | T | C | 2 | a0001c0004 a0001c0012 |
19 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(16): Show |
synonymous_variant | LOW | c.1893A>G | p.Thr631Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1955/5704 | 1893/1986 | 631/661 | chr3 | 134603672 | |||
| chr3:134603831 | G | A | 1 | a0001c0012 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1796/5704 | 1734/1986 | 578/661 | chr3 | 134603831 | |||
| chr3:134603900 | A | G | 5 | a0001c0001 a0001c0004 a0001c0006 others(2): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
synonymous_variant | LOW | c.1665T>C | p.Leu555Leu | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1727/5704 | 1665/1986 | 555/661 | chr3 | 134603900 | |||
| chr3:134603972 | G | C | 6 | a0001c0002 a0001c0003 a0001c0007 others(3): Show |
97 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(94): Show |
synonymous_variant | LOW | c.1593C>G | p.Gly531Gly | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1655/5704 | 1593/1986 | 531/661 | chr3 | 134603972 | |||
| chr3:134604002 | G | A | 1 | a0001c0007 | 3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.1563C>T | p.Thr521Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1625/5704 | 1563/1986 | 521/661 | chr3 | 134604002 | |||
| chr3:134604074 | G | A | 1 | a0001c0008 | 3 | HG02056.hp2 NA18956.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.1491C>T | p.His497His | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1553/5704 | 1491/1986 | 497/661 | chr3 | 134604074 | |||
| chr3:134604314 | A | G | 13 | a0001c0001 a0001c0002 a0001c0003 others(10): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
synonymous_variant | LOW | c.1251T>C | p.Phe417Phe | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1313/5704 | 1251/1986 | 417/661 | chr3 | 134604314 | |||
| chr3:134650874 | C | A | 4 | a0001c0003 a0001c0006 a0002c0010 others(1): Show |
44 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.87G>T | p.Thr29Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/11 | 149/5704 | 87/1986 | 29/661 | chr3 | 134650874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134600000 | G | A | 1 | a0004c0014t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3579 | chr3 | 134600000 | ||||||
| chr3:134600007 | A | G | 3 | a0001c0002t0004 a0001c0002t0015 a0001c0002t0020 |
15 | HG02922.hp2 HG03041.hp1 NA18941.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3572T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3572 | chr3 | 134600007 | ||||||
| chr3:134600130 | G | A | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3449C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3449 | chr3 | 134600130 | ||||||
| chr3:134600606 | C | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2973G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2973 | chr3 | 134600606 | ||||||
| chr3:134600613 | C | T | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2966G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2966 | chr3 | 134600613 | ||||||
| chr3:134600715 | T | C | 1 | a0001c0001t0008 | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2864A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2864 | chr3 | 134600715 | ||||||
| chr3:134600881 | T | A | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2698A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2698 | chr3 | 134600881 | ||||||
| chr3:134600908 | C | G | 1 | a0001c0001t0005 | 10 | HG00558.hp2 HG01255.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2671G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2671 | chr3 | 134600908 | ||||||
| chr3:134601018 | C | T | 1 | a0001c0001t0022 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2561 | chr3 | 134601018 | ||||||
| chr3:134601262 | GA | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2316delT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2316 | chr3 | 134601262 | ||||||
| chr3:134601451 | T | C | 1 | a0001c0001t0023 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2128A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2128 | chr3 | 134601451 | ||||||
| chr3:134601462 | C | T | 1 | a0001c0001t0014 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2117 | chr3 | 134601462 | ||||||
| chr3:134601540 | C | T | 1 | a0001c0001t0012 | 2 | HG01952.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2039G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2039 | chr3 | 134601540 | ||||||
| chr3:134601657 | G | A | 1 | a0001c0001t0013 | 2 | HG02735.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1922C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1922 | chr3 | 134601657 | ||||||
| chr3:134601737 | C | T | 1 | a0001c0002t0019 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1842G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1842 | chr3 | 134601737 | ||||||
| chr3:134601923 | A | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1656T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1656 | chr3 | 134601923 | ||||||
| chr3:134601983 | T | TTACCAAG others(4): Show |
36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(33): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*1595_*1596insGTGC others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1595 | chr3 | 134601983 | ||||||
| chr3:134602161 | C | T | 3 | a0001c0001t0003 a0001c0001t0027 a0001c0006t0003 |
16 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1418 | chr3 | 134602161 | ||||||
| chr3:134602220 | CAGTGGCC others(4): Show |
C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348_*1358delACAT others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1348 | chr3 | 134602220 | ||||||
| chr3:134602229 | T | C | 1 | a0001c0005t0016 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1350 | chr3 | 134602229 | ||||||
| chr3:134602240 | T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1339A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1339 | chr3 | 134602240 | ||||||
| chr3:134602244 | G | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1335 | chr3 | 134602244 | ||||||
| chr3:134602245 | C | T | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1334 | chr3 | 134602245 | ||||||
| chr3:134602247 | T | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1332 | chr3 | 134602247 | ||||||
| chr3:134602249 | T | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1330 | chr3 | 134602249 | ||||||
| chr3:134602253 | T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1326A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1326 | chr3 | 134602253 | ||||||
| chr3:134602255 | T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1324 | chr3 | 134602255 | ||||||
| chr3:134602256 | T | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1323A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1323 | chr3 | 134602256 | ||||||
| chr3:134602280 | T | G | 1 | a0001c0005t0007 | 5 | HG01109.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1299A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1299 | chr3 | 134602280 | ||||||
| chr3:134602288 | G | A | 1 | a0001c0004t0011 | 3 | HG01891.hp1 HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1291C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1291 | chr3 | 134602288 | ||||||
| chr3:134602310 | G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1269C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1269 | chr3 | 134602310 | ||||||
| chr3:134602313 | G | T | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1266 | chr3 | 134602313 | ||||||
| chr3:134602314 | C | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1265G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1265 | chr3 | 134602314 | ||||||
| chr3:134602315 | G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1264 | chr3 | 134602315 | ||||||
| chr3:134602317 | T | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1262 | chr3 | 134602317 | ||||||
| chr3:134602318 | G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1261 | chr3 | 134602318 | ||||||
| chr3:134602572 | G | A | 2 | a0001c0002t0021 a0001c0007t0010 |
4 | HG01123.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1007 | chr3 | 134602572 | ||||||
| chr3:134602681 | T | C | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*898A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 898 | chr3 | 134602681 | ||||||
| chr3:134602738 | A | C | 2 | a0001c0005t0006 a0001c0005t0016 |
9 | HG02723.hp2 HG02818.hp1 NA18951.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*841T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 841 | chr3 | 134602738 | ||||||
| chr3:134602757 | G | A | 1 | a0001c0002t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 822 | chr3 | 134602757 | ||||||
| chr3:134602824 | G | C | 1 | a0001c0001t0024 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 755 | chr3 | 134602824 | ||||||
| chr3:134602827 | T | A | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(16): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*752A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 752 | chr3 | 134602827 | ||||||
| chr3:134602909 | C | T | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*670G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 670 | chr3 | 134602909 | ||||||
| chr3:134602936 | G | C | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 643 | chr3 | 134602936 | ||||||
| chr3:134602966 | G | A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*613C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 613 | chr3 | 134602966 | ||||||
| chr3:134602986 | T | C | 1 | a0001c0006t0026 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 593 | chr3 | 134602986 | ||||||
| chr3:134603166 | A | T | 1 | a0001c0001t0029 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 413 | chr3 | 134603166 | ||||||
| chr3:134603207 | T | C | 1 | a0001c0001t0027 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 372 | chr3 | 134603207 | ||||||
| chr3:134603271 | G | A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 308 | chr3 | 134603271 | ||||||
| chr3:134603321 | C | A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 258 | chr3 | 134603321 | ||||||
| chr3:134603375 | C | G | 1 | a0001c0005t0007 | 5 | HG01109.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 204 | chr3 | 134603375 | ||||||
| chr3:134603377 | C | A | 1 | a0001c0012t0028 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 202 | chr3 | 134603377 | ||||||
| chr3:134603404 | G | C | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 175 | chr3 | 134603404 | ||||||
| chr3:134603405 | C | G | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 174 | chr3 | 134603405 | ||||||
| chr3:134603442 | G | A | 1 | a0001c0001t0029 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 137 | chr3 | 134603442 | ||||||
| chr3:134603578 | C | T | 1 | a0001c0001t0014 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1 | chr3 | 134603578 | ||||||
| chr3:134651016 | T | C | 1 | a0001c0002t0030 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/11 | 56 | chr3 | 134651016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134604597 | C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1091-123G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604597 | |||||||
| chr3:134604680 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-206C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604680 | |||||||
| chr3:134604733 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1091-259G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604733 | |||||||
| chr3:134604779 | C | G | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-305G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604779 | |||||||
| chr3:134604868 | T | C | 1 | a0001c0005t0006g0159 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1091-394A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604868 | |||||||
| chr3:134604977 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-503A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604977 | |||||||
| chr3:134605042 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1091-568C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605042 | |||||||
| chr3:134605182 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-708C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605182 | |||||||
| chr3:134605212 | G | A | 2 | a0001c0005t0007g0046 a0001c0005t0007g0048 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1091-738C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605212 | |||||||
| chr3:134605267 | G | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0152 |
5 | HG00609.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-793C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605267 | |||||||
| chr3:134605378 | G | A | 9 | a0001c0003t0002g0219 a0001c0003t0002g0222 a0001c0003t0002g0223 others(6): Show |
9 | NA18939.hp2 NA18956.hp1 NA18989.hp1 others(6): Show |
intron_variant | MODIFIER | c.1091-904C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605378 | |||||||
| chr3:134605435 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1091-961C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605435 | |||||||
| chr3:134605761 | C | T | 1 | a0005c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1091-1287G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605761 | |||||||
| chr3:134605762 | G | A | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1091-1288C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605762 | |||||||
| chr3:134606414 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-1940A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606414 | |||||||
| chr3:134606484 | G | A | 3 | a0001c0002t0021g0060 a0001c0007t0010g0015 a0001c0007t0010g0083 |
4 | HG01123.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-2010C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606484 | |||||||
| chr3:134606527 | C | A | 1 | a0005c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1091-2053G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606527 | |||||||
| chr3:134606665 | C | T | 3 | a0001c0002t0002g0113 a0001c0002t0002g0114 a0001c0002t0002g0120 |
3 | HG00099.hp1 HG02683.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1090+1984G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606665 | |||||||
| chr3:134606686 | G | A | 1 | a0004c0014t0017g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1090+1963C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606686 | |||||||
| chr3:134606694 | G | A | 85 | a0001c0002t0002g0006 a0001c0002t0002g0012 a0001c0002t0002g0029 others(82): Show |
97 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1090+1955C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606694 | |||||||
| chr3:134606784 | A | G | 79 | a0001c0002t0002g0006 a0001c0002t0002g0012 a0001c0002t0002g0029 others(76): Show |
90 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1090+1865T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606784 | |||||||
| chr3:134606815 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1090+1834A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606815 | |||||||
| chr3:134606895 | T | C | 1 | a0001c0003t0002g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1090+1754A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606895 | |||||||
| chr3:134607139 | C | T | 2 | a0001c0001t0005g0019 a0001c0001t0005g0139 |
3 | HG02523.hp1 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1090+1510G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607139 | |||||||
| chr3:134607151 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1090+1498C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607151 | |||||||
| chr3:134607225 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0078 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+1424G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607225 | |||||||
| chr3:134607306 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1090+1343A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607306 | |||||||
| chr3:134607420 | C | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0069 a0001c0001t0003g0096 |
4 | HG00323.hp1 HG02300.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+1229G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607420 | |||||||
| chr3:134607483 | G | A | 10 | a0001c0002t0004g0004 a0001c0002t0004g0034 a0001c0002t0004g0035 others(7): Show |
13 | NA18941.hp1 NA18955.hp2 NA18960.hp1 others(10): Show |
intron_variant | MODIFIER | c.1090+1166C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607483 | |||||||
| chr3:134607693 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1090+956T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607693 | |||||||
| chr3:134607768 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0030 others(51): Show |
72 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1090+881C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607768 | |||||||
| chr3:134607784 | G | A | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+865C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607784 | |||||||
| chr3:134607842 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1090+807C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607842 | |||||||
| chr3:134608640 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0181 |
2 | HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1090+9G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134608640 | |||||||
| chr3:134608913 | G | T | 8 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0158 others(5): Show |
8 | HG02818.hp1 NA18951.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-74C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134608913 | |||||||
| chr3:134608953 | G | T | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-114C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134608953 | |||||||
| chr3:134609088 | G | A | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900-249C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609088 | |||||||
| chr3:134609137 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.900-298C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609137 | |||||||
| chr3:134609196 | G | A | 9 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0158 others(6): Show |
9 | HG02723.hp2 HG02818.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.900-357C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609196 | |||||||
| chr3:134609368 | G | C | 1 | a0001c0002t0002g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.900-529C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609368 | |||||||
| chr3:134609464 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-625A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609464 | |||||||
| chr3:134609491 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.900-652T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609491 | |||||||
| chr3:134609496 | T | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.900-657A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609496 | |||||||
| chr3:134609519 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+676G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609519 | |||||||
| chr3:134609654 | C | T | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+541G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609654 | |||||||
| chr3:134609832 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.899+363C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609832 | |||||||
| chr3:134609898 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+297T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609898 | |||||||
| chr3:134610022 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+173G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610022 | |||||||
| chr3:134610129 | A | G | 2 | a0001c0002t0002g0006 a0001c0002t0002g0152 |
5 | HG00609.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.899+66T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610129 | |||||||
| chr3:134610166 | C | T | 1 | a0001c0005t0016g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.899+29G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610166 | |||||||
| chr3:134610176 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.899+19T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610176 | |||||||
| chr3:134610414 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.711-31C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610414 | |||||||
| chr3:134610495 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.711-112T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610495 | |||||||
| chr3:134610551 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.711-168C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610551 | |||||||
| chr3:134610693 | G | A | 84 | a0001c0001t0001g0116 a0001c0002t0002g0006 a0001c0002t0002g0012 others(81): Show |
95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-310C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610693 | |||||||
| chr3:134610734 | C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.711-351G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610734 | |||||||
| chr3:134610758 | G | A | 84 | a0001c0001t0001g0116 a0001c0002t0002g0006 a0001c0002t0002g0012 others(81): Show |
95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-375C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610758 | |||||||
| chr3:134610799 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.711-416A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610799 | |||||||
| chr3:134610979 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-596C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610979 | |||||||
| chr3:134610994 | C | G | 27 | a0001c0002t0002g0062 a0001c0002t0002g0067 a0001c0002t0002g0107 others(24): Show |
31 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.711-611G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610994 | |||||||
| chr3:134611185 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-802G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611185 | |||||||
| chr3:134611200 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0026 a0001c0004t0001g0202 |
6 | HG02922.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-817C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611200 | |||||||
| chr3:134611241 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-858G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611241 | |||||||
| chr3:134611249 | G | T | 1 | a0001c0001t0027g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.711-866C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611249 | |||||||
| chr3:134611371 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-988G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611371 | |||||||
| chr3:134611477 | C | T | 1 | a0001c0001t0024g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.711-1094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611477 | |||||||
| chr3:134611532 | T | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1149A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611532 | |||||||
| chr3:134611602 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.711-1219C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611602 | |||||||
| chr3:134611770 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1387G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611770 | |||||||
| chr3:134611867 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1484A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611867 | |||||||
| chr3:134611912 | C | A | 1 | a0001c0002t0004g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.711-1529G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611912 | |||||||
| chr3:134612134 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1751A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612134 | |||||||
| chr3:134612137 | C | T | 4 | a0001c0005t0007g0046 a0001c0005t0007g0047 a0001c0005t0007g0048 others(1): Show |
4 | HG02572.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-1754G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612137 | |||||||
| chr3:134612196 | G | A | 7 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0026 others(4): Show |
12 | HG01167.hp2 HG01169.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.711-1813C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612196 | |||||||
| chr3:134612200 | T | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0030 others(39): Show |
53 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-1817A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612200 | |||||||
| chr3:134612206 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1823T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612206 | |||||||
| chr3:134612246 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.711-1863C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612246 | |||||||
| chr3:134612325 | C | T | 84 | a0001c0001t0001g0116 a0001c0002t0002g0006 a0001c0002t0002g0012 others(81): Show |
95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-1942G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612325 | |||||||
| chr3:134612362 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.711-1979C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612362 | |||||||
| chr3:134612624 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2241T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612624 | |||||||
| chr3:134612684 | C | A | 1 | a0001c0002t0002g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.711-2301G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612684 | |||||||
| chr3:134612751 | C | CTG | 43 | a0001c0001t0001g0091 a0001c0001t0001g0116 a0001c0001t0001g0198 others(40): Show |
50 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.711-2370_711-2369d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTG | 27 | a0001c0001t0001g0056 a0001c0001t0001g0134 a0001c0001t0001g0138 others(24): Show |
34 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.711-2372_711-2369d others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTGTG | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
57 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.711-2374_711-2369d others(8): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTGTGT others(1): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(26): Show |
41 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.711-2376_711-2369d others(10): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTGTGT others(3): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0077 others(16): Show |
26 | HG00280.hp1 HG00544.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.711-2378_711-2369d others(12): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTGTGT others(5): Show |
8 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
8 | HG01109.hp2 HG01261.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2380_711-2369d others(14): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0005t0007g0033 |
4 | HG01109.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2382_711-2369d others(16): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | CTG | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0084 others(4): Show |
7 | HG01099.hp2 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.711-2370_711-2369d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612751 | CTGTGTGT others(13): Show |
C | 5 | a0001c0002t0004g0004 a0001c0002t0004g0041 a0001c0002t0004g0044 others(2): Show |
8 | NA18960.hp1 NA18965.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2388_711-2369d others(22): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | |||||||
| chr3:134612756 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.711-2384_711-2374d others(13): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612756 | |||||||
| chr3:134612795 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.711-2413_711-2412i others(17): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612795 | |||||||
| chr3:134613032 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.711-2649A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613032 | |||||||
| chr3:134613138 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2755G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613138 | |||||||
| chr3:134613308 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.711-2925C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613308 | |||||||
| chr3:134613309 | T | C | 4 | a0001c0005t0007g0046 a0001c0005t0007g0047 a0001c0005t0007g0048 others(1): Show |
4 | HG02572.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-2926A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613309 | |||||||
| chr3:134613380 | C | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2997G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613380 | |||||||
| chr3:134613407 | G | A | 1 | a0001c0005t0006g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.711-3024C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613407 | |||||||
| chr3:134613417 | C | T | 3 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0175 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.711-3034G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613417 | |||||||
| chr3:134613455 | C | T | 1 | a0001c0001t0005g0154 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.711-3072G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613455 | |||||||
| chr3:134613469 | G | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3086C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613469 | |||||||
| chr3:134613477 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613477 | |||||||
| chr3:134613921 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0069 a0001c0001t0003g0096 |
4 | HG00323.hp1 HG02300.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-3538G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613921 | |||||||
| chr3:134613934 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3551A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613934 | |||||||
| chr3:134614062 | T | C | 1 | a0001c0002t0002g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.711-3679A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614062 | |||||||
| chr3:134614084 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3701T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614084 | |||||||
| chr3:134614319 | C | T | 88 | a0001c0001t0001g0116 a0001c0002t0002g0006 a0001c0002t0002g0012 others(85): Show |
99 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.711-3936G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614319 | |||||||
| chr3:134614612 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.711-4229C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614612 | |||||||
| chr3:134614869 | C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.710+4279G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614869 | |||||||
| chr3:134614870 | G | A | 8 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0158 others(5): Show |
8 | HG02818.hp1 NA18951.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+4278C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614870 | |||||||
| chr3:134614932 | G | C | 1 | a0001c0002t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.710+4216C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614932 | |||||||
| chr3:134615283 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.710+3865C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615283 | |||||||
| chr3:134615306 | G | A | 11 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0175 others(8): Show |
11 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.710+3842C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615306 | |||||||
| chr3:134615349 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.710+3798dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | |||||||
| chr3:134615349 | C | CTT | 6 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0022g0136 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+3797_710+3798d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | |||||||
| chr3:134615349 | CT | C | 16 | a0001c0002t0002g0012 a0001c0002t0002g0058 a0001c0002t0002g0118 others(13): Show |
17 | HG02615.hp2 HG02622.hp2 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+3798delA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | |||||||
| chr3:134615394 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.710+3754T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615394 | |||||||
| chr3:134615469 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.710+3679T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615469 | |||||||
| chr3:134615485 | G | A | 97 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0006 others(94): Show |
108 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.710+3663C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615485 | |||||||
| chr3:134615530 | C | T | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3618G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615530 | |||||||
| chr3:134615531 | ACCAGCTC others(164): Show |
A | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3446_710+3616d others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615531 | |||||||
| chr3:134615605 | G | A | 7 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0158 others(4): Show |
7 | NA18951.hp1 NA18960.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+3543C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615605 | |||||||
| chr3:134615622 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.710+3526G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615622 | |||||||
| chr3:134615671 | G | A | 88 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0006 others(85): Show |
99 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.710+3477C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615671 | |||||||
| chr3:134615678 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3470T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615678 | |||||||
| chr3:134615680 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3468C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615680 | |||||||
| chr3:134615682 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3466A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615682 | |||||||
| chr3:134615704 | C | A | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3444G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615704 | |||||||
| chr3:134615705 | A | T | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3443T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615705 | |||||||
| chr3:134615707 | C | A | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3441G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615707 | |||||||
| chr3:134615787 | T | G | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710+3361A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615787 | |||||||
| chr3:134615896 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.710+3252C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615896 | |||||||
| chr3:134616015 | G | A | 1 | a0001c0001t0023g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.710+3133C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616015 | |||||||
| chr3:134616082 | G | A | 3 | a0001c0004t0001g0145 a0001c0004t0001g0146 a0001c0004t0001g0149 |
3 | HG02809.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.710+3066C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616082 | |||||||
| chr3:134616132 | C | T | 2 | a0001c0001t0014g0052 a0001c0006t0026g0207 |
2 | HG02683.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.710+3016G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616132 | |||||||
| chr3:134616133 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.710+3015T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616133 | |||||||
| chr3:134616192 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.710+2956A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616192 | |||||||
| chr3:134616412 | C | T | 1 | a0001c0005t0006g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.710+2736G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616412 | |||||||
| chr3:134616629 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.710+2519A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616629 | |||||||
| chr3:134616684 | T | G | 3 | a0001c0002t0021g0060 a0001c0004t0001g0173 a0001c0004t0001g0174 |
3 | HG02622.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2464A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616684 | |||||||
| chr3:134616763 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0078 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+2385A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616763 | |||||||
| chr3:134616806 | G | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710+2342C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616806 | |||||||
| chr3:134617132 | C | T | 3 | a0001c0002t0021g0060 a0001c0004t0001g0173 a0001c0004t0001g0174 |
3 | HG02622.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2016G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617132 | |||||||
| chr3:134617151 | T | C | 86 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0001t0001g0150 others(83): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710+1997A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617151 | |||||||
| chr3:134617167 | A | T | 1 | a0001c0003t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.710+1981T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617167 | |||||||
| chr3:134617253 | A | T | 84 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0006 others(81): Show |
97 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.710+1895T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617253 | |||||||
| chr3:134617262 | C | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0080 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.710+1886G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617262 | |||||||
| chr3:134617524 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.710+1624G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617524 | |||||||
| chr3:134617720 | G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710+1428C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617720 | |||||||
| chr3:134617813 | G | A | 1 | a0001c0006t0003g0028 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.710+1335C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617813 | |||||||
| chr3:134617962 | C | T | 1 | a0001c0003t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.710+1186G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617962 | |||||||
| chr3:134618010 | G | C | 1 | a0001c0002t0002g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.710+1138C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618010 | |||||||
| chr3:134618054 | C | T | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.710+1094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618054 | |||||||
| chr3:134618055 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.710+1093G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618055 | |||||||
| chr3:134618092 | C | A | 1 | a0001c0004t0001g0010 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.710+1056G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618092 | |||||||
| chr3:134618114 | T | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.710+1034A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618114 | |||||||
| chr3:134618199 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.710+949C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618199 | |||||||
| chr3:134618298 | G | A | 1 | a0001c0003t0002g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.710+850C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618298 | |||||||
| chr3:134618434 | T | A | 10 | a0001c0002t0002g0006 a0001c0002t0002g0152 a0001c0005t0006g0104 others(7): Show |
13 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.710+714A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618434 | |||||||
| chr3:134618762 | C | A | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.710+386G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618762 | |||||||
| chr3:134618881 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.710+267G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618881 | |||||||
| chr3:134619023 | G | A | 4 | a0001c0002t0002g0059 a0001c0002t0002g0123 a0001c0002t0002g0124 others(1): Show |
4 | HG01243.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+125C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134619023 | |||||||
| chr3:134619324 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0108 others(3): Show |
8 | HG00741.hp1 HG02109.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.593-59G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619324 | |||||||
| chr3:134619346 | G | A | 1 | a0001c0006t0001g0208 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.593-81C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619346 | |||||||
| chr3:134619543 | G | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593-278C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619543 | |||||||
| chr3:134619640 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0099 others(6): Show |
13 | HG01934.hp2 HG02074.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.593-375A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619640 | |||||||
| chr3:134619696 | C | T | 1 | a0001c0001t0005g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.593-431G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619696 | |||||||
| chr3:134619746 | T | C | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.593-481A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619746 | |||||||
| chr3:134619788 | T | C | 4 | a0001c0004t0001g0145 a0001c0004t0001g0146 a0001c0004t0001g0147 others(1): Show |
4 | HG02809.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-523A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619788 | |||||||
| chr3:134619927 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.593-662T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619927 | |||||||
| chr3:134620260 | C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592+489G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620260 | |||||||
| chr3:134620312 | C | T | 1 | a0001c0003t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.592+437G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620312 | |||||||
| chr3:134620527 | G | A | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.592+222C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620527 | |||||||
| chr3:134620896 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0025g0170 |
3 | HG03831.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.484-39C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134620896 | |||||||
| chr3:134620948 | C | G | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.484-91G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134620948 | |||||||
| chr3:134621037 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0101 |
4 | HG00099.hp2 HG00323.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-180G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621037 | |||||||
| chr3:134621125 | A | C | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-268T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621125 | |||||||
| chr3:134621219 | C | T | 1 | a0001c0001t0003g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.484-362G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621219 | |||||||
| chr3:134621421 | C | T | 1 | a0001c0006t0001g0208 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.484-564G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621421 | |||||||
| chr3:134621437 | G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.484-580C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621437 | |||||||
| chr3:134621511 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.484-654G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621511 | |||||||
| chr3:134621592 | A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.484-735T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621592 | |||||||
| chr3:134621637 | C | A | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.484-780G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621637 | |||||||
| chr3:134621700 | G | GA | 4 | a0001c0001t0001g0161 a0001c0002t0002g0049 a0001c0002t0002g0050 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-844dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621700 | |||||||
| chr3:134621724 | G | A | 1 | a0001c0001t0005g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484-867C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621724 | |||||||
| chr3:134622008 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.484-1151T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622008 | |||||||
| chr3:134622218 | A | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.484-1361T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622218 | |||||||
| chr3:134622265 | A | G | 2 | a0001c0001t0001g0064 a0001c0006t0001g0218 |
2 | HG01069.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.484-1408T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622265 | |||||||
| chr3:134622381 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.484-1524G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622381 | |||||||
| chr3:134622455 | G | A | 5 | a0001c0002t0002g0062 a0001c0002t0002g0107 a0001c0003t0002g0007 others(2): Show |
8 | HG01175.hp2 HG01261.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-1598C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622455 | |||||||
| chr3:134622543 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0084 |
3 | HG01496.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.484-1686G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622543 | |||||||
| chr3:134622723 | G | A | 2 | a0001c0005t0006g0166 a0001c0006t0003g0235 |
2 | HG02723.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.484-1866C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622723 | |||||||
| chr3:134622793 | A | G | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.484-1936T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622793 | |||||||
| chr3:134622866 | C | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.484-2009G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622866 | |||||||
| chr3:134623285 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.483+1768G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623285 | |||||||
| chr3:134623345 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.483+1708A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623345 | |||||||
| chr3:134623551 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.483+1502G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623551 | |||||||
| chr3:134623756 | T | A | 3 | a0001c0002t0002g0111 a0001c0002t0002g0112 a0001c0002t0002g0172 |
3 | HG02055.hp2 HG03098.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.483+1297A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623756 | |||||||
| chr3:134623760 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.483+1293C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623760 | |||||||
| chr3:134623836 | G | A | 4 | a0001c0002t0002g0059 a0001c0002t0002g0123 a0001c0002t0002g0124 others(1): Show |
4 | HG01243.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1217C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623836 | |||||||
| chr3:134623916 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.483+1137A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623916 | |||||||
| chr3:134623916 | T | G | 1 | a0001c0006t0003g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.483+1137A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623916 | |||||||
| chr3:134624226 | G | T | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.483+827C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624226 | |||||||
| chr3:134624246 | C | T | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483+807G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624246 | |||||||
| chr3:134624372 | T | A | 1 | a0001c0003t0002g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.483+681A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624372 | |||||||
| chr3:134624710 | G | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483+343C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624710 | |||||||
| chr3:134624798 | G | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483+255C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624798 | |||||||
| chr3:134624846 | C | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.483+207G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624846 | |||||||
| chr3:134625032 | C | G | 2 | a0001c0001t0013g0189 a0001c0001t0013g0190 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.483+21G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134625032 | |||||||
| chr3:134625215 | A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.401-80T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625215 | |||||||
| chr3:134625340 | C | T | 80 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0012 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.401-205G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625340 | |||||||
| chr3:134625488 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.401-353C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625488 | |||||||
| chr3:134625593 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.401-458G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625593 | |||||||
| chr3:134625663 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.401-528C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625663 | |||||||
| chr3:134625683 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.401-548C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625683 | |||||||
| chr3:134625852 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.401-717T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625852 | |||||||
| chr3:134625876 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.401-741C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625876 | |||||||
| chr3:134625882 | C | T | 2 | a0001c0002t0002g0029 a0001c0005t0007g0033 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.401-747G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625882 | |||||||
| chr3:134625938 | C | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.401-803G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625938 | |||||||
| chr3:134625957 | G | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.401-822C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625957 | |||||||
| chr3:134625966 | T | C | 1 | a0001c0001t0008g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.401-831A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625966 | |||||||
| chr3:134625997 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.401-862C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625997 | |||||||
| chr3:134626053 | A | G | 1 | a0001c0003t0002g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.401-918T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626053 | |||||||
| chr3:134626086 | T | G | 83 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0012 others(80): Show |
93 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.401-951A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626086 | |||||||
| chr3:134626090 | C | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01109.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-955G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626090 | |||||||
| chr3:134626114 | C | T | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-979G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626114 | |||||||
| chr3:134626306 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.401-1171A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626306 | |||||||
| chr3:134626472 | G | A | 1 | a0001c0004t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+1284C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626472 | |||||||
| chr3:134626485 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+1271G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626485 | |||||||
| chr3:134626555 | G | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+1201C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626555 | |||||||
| chr3:134626746 | C | A | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+1010G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626746 | |||||||
| chr3:134626842 | T | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.400+914A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626842 | |||||||
| chr3:134626877 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.400+879G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626877 | |||||||
| chr3:134626882 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+874A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626882 | |||||||
| chr3:134626939 | A | C | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+817T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626939 | |||||||
| chr3:134626946 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+810A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626946 | |||||||
| chr3:134627183 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+573C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627183 | |||||||
| chr3:134627265 | G | C | 1 | a0001c0001t0005g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.400+491C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627265 | |||||||
| chr3:134627296 | C | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.400+460G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627296 | |||||||
| chr3:134627375 | C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+381G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627375 | |||||||
| chr3:134627473 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0110 a0001c0001t0005g0140 others(2): Show |
6 | HG00558.hp2 HG01255.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+283C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627473 | |||||||
| chr3:134627480 | G | A | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+276C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627480 | |||||||
| chr3:134627518 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.400+238A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627518 | |||||||
| chr3:134627525 | G | C | 3 | a0001c0002t0002g0111 a0001c0002t0002g0112 a0001c0002t0002g0172 |
3 | HG02055.hp2 HG03098.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.400+231C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627525 | |||||||
| chr3:134627839 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.338-21C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134627839 | |||||||
| chr3:134627920 | C | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.338-102G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134627920 | |||||||
| chr3:134628123 | C | A | 2 | a0001c0001t0013g0189 a0001c0001t0013g0190 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.338-305G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628123 | |||||||
| chr3:134628148 | G | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.338-330C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628148 | |||||||
| chr3:134628211 | A | G | 1 | a0001c0002t0002g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.338-393T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628211 | |||||||
| chr3:134628619 | C | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.338-801G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628619 | |||||||
| chr3:134628644 | G | A | 2 | a0001c0006t0003g0028 a0001c0006t0003g0236 |
3 | HG00642.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.338-826C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628644 | |||||||
| chr3:134628651 | T | C | 1 | a0001c0001t0023g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.338-833A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628651 | |||||||
| chr3:134628742 | C | T | 12 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(9): Show |
15 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(12): Show |
intron_variant | MODIFIER | c.337+879G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628742 | |||||||
| chr3:134628809 | G | C | 1 | a0001c0001t0027g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.337+812C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628809 | |||||||
| chr3:134628816 | C | G | 1 | a0001c0001t0003g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.337+805G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628816 | |||||||
| chr3:134629034 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.337+587G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134629034 | |||||||
| chr3:134629434 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.337+187G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134629434 | |||||||
| chr3:134629796 | C | A | 19 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0090 others(16): Show |
19 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.263-101G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629796 | |||||||
| chr3:134629895 | G | T | 1 | a0001c0002t0021g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-200C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629895 | |||||||
| chr3:134629952 | A | C | 2 | a0001c0001t0001g0150 a0001c0006t0001g0011 |
4 | HG02109.hp1 HG03225.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-257T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629952 | |||||||
| chr3:134629954 | G | A | 27 | a0001c0002t0002g0062 a0001c0002t0002g0107 a0001c0002t0002g0122 others(24): Show |
31 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.263-259C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629954 | |||||||
| chr3:134630088 | T | G | 80 | a0001c0001t0001g0032 a0001c0001t0001g0116 a0001c0002t0002g0012 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-393A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630088 | |||||||
| chr3:134630363 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.263-668T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630363 | |||||||
| chr3:134630403 | G | GT | 82 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(79): Show |
92 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.263-709dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630403 | |||||||
| chr3:134630505 | G | A | 5 | a0001c0002t0002g0029 a0001c0002t0002g0049 a0001c0002t0002g0050 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-810C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630505 | |||||||
| chr3:134630868 | G | C | 80 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-1173C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630868 | |||||||
| chr3:134631041 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.263-1346C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631041 | |||||||
| chr3:134631153 | G | A | 80 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-1458C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631153 | |||||||
| chr3:134631387 | C | T | 2 | a0001c0002t0002g0029 a0001c0005t0007g0033 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.263-1692G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631387 | |||||||
| chr3:134631404 | G | A | 2 | a0001c0003t0002g0211 a0001c0003t0002g0215 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.263-1709C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631404 | |||||||
| chr3:134631545 | TTTTGATA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.263-1857_263-1851d others(9): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631545 | |||||||
| chr3:134631877 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.263-2182C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631877 | |||||||
| chr3:134631914 | A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-2219T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631914 | |||||||
| chr3:134631929 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-2234G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631929 | |||||||
| chr3:134632072 | C | G | 1 | a0001c0002t0002g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.263-2377G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632072 | |||||||
| chr3:134632170 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.263-2475G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632170 | |||||||
| chr3:134632181 | C | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG01243.hp2 HG01496.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-2486G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632181 | |||||||
| chr3:134632302 | C | A | 2 | a0001c0003t0002g0220 a0001c0003t0002g0221 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.263-2607G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632302 | |||||||
| chr3:134632308 | G | A | 2 | a0001c0003t0002g0216 a0001c0003t0002g0228 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.263-2613C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632308 | |||||||
| chr3:134632456 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.263-2761C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632456 | |||||||
| chr3:134632489 | C | T | 1 | a0001c0003t0002g0230 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.263-2794G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632489 | |||||||
| chr3:134632882 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.263-3187T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632882 | |||||||
| chr3:134632923 | G | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-3228C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632923 | |||||||
| chr3:134632941 | C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.263-3246G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632941 | |||||||
| chr3:134633124 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-3429A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633124 | |||||||
| chr3:134633363 | C | T | 1 | a0001c0004t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.263-3668G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633363 | |||||||
| chr3:134633379 | A | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.263-3684T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633379 | |||||||
| chr3:134633502 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.263-3807T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633502 | |||||||
| chr3:134633556 | G | A | 3 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0175 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.263-3861C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633556 | |||||||
| chr3:134633592 | A | G | 1 | a0001c0003t0002g0222 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.263-3897T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633592 | |||||||
| chr3:134633817 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-4122A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633817 | |||||||
| chr3:134633912 | G | A | 11 | a0001c0002t0002g0012 a0001c0002t0002g0037 a0001c0002t0002g0057 others(8): Show |
12 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-4217C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633912 | |||||||
| chr3:134633924 | T | C | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.263-4229A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633924 | |||||||
| chr3:134633933 | A | C | 1 | a0001c0001t0003g0096 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.263-4238T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633933 | |||||||
| chr3:134634070 | C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-4375G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634070 | |||||||
| chr3:134634200 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.263-4505T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634200 | |||||||
| chr3:134634443 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.263-4748T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634443 | |||||||
| chr3:134634532 | T | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-4837A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634532 | |||||||
| chr3:134635040 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.263-5345G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635040 | |||||||
| chr3:134635143 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.263-5448T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635143 | |||||||
| chr3:134635246 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.263-5551G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635246 | |||||||
| chr3:134635412 | G | A | 1 | a0001c0001t0029g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.263-5717C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635412 | |||||||
| chr3:134635429 | G | A | 1 | a0001c0003t0002g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.263-5734C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635429 | |||||||
| chr3:134635445 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.263-5750G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635445 | |||||||
| chr3:134635493 | T | TA | 5 | a0001c0003t0002g0220 a0001c0003t0002g0231 a0001c0005t0006g0166 others(2): Show |
6 | HG01123.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.263-5799dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635493 | T | TAA | 73 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0116 others(70): Show |
83 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.263-5800_263-5799d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635493 | T | TAAA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0030 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.263-5801_263-5799d others(5): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635493 | T | TAAAA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(52): Show |
77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.263-5802_263-5799d others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635493 | T | TAAAAA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0101 a0001c0001t0001g0142 others(3): Show |
7 | HG00735.hp1 HG01175.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-5803_263-5799d others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635493 | T | TTAAA | 3 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0175 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.263-5799_263-5798i others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | |||||||
| chr3:134635532 | A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-5837T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635532 | |||||||
| chr3:134636216 | T | A | 2 | a0001c0007t0010g0015 a0001c0007t0010g0083 |
3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.263-6521A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636216 | |||||||
| chr3:134636236 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(52): Show |
78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.263-6541G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636236 | |||||||
| chr3:134636272 | C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.263-6577G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636272 | |||||||
| chr3:134636347 | G | T | 80 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-6652C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636347 | |||||||
| chr3:134636589 | C | T | 11 | a0001c0001t0014g0052 a0001c0002t0002g0006 a0001c0002t0002g0152 others(8): Show |
14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.262+6727G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636589 | |||||||
| chr3:134636655 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.262+6661T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636655 | |||||||
| chr3:134636691 | C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262+6625G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636691 | |||||||
| chr3:134636828 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+6488A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636828 | |||||||
| chr3:134637900 | A | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0002t0004g0004 others(9): Show |
15 | HG02922.hp2 HG03041.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.262+5416T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134637900 | |||||||
| chr3:134637928 | C | T | 2 | a0001c0002t0030g0239 a0001c0004t0011g0008 |
4 | HG01255.hp2 HG01891.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+5388G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134637928 | |||||||
| chr3:134638895 | C | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+4421G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638895 | |||||||
| chr3:134638907 | GGT | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.262+4407_262+4408d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638907 | |||||||
| chr3:134638939 | C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.262+4377G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638939 | |||||||
| chr3:134638990 | A | G | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG01243.hp2 HG01496.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+4326T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638990 | |||||||
| chr3:134639047 | C | CT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.262+4268dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639047 | |||||||
| chr3:134639061 | T | G | 1 | a0001c0005t0007g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.262+4255A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639061 | |||||||
| chr3:134639070 | G | GT | 15 | a0001c0001t0001g0150 a0001c0001t0014g0052 a0001c0002t0002g0006 others(12): Show |
18 | HG00609.hp2 HG02109.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.262+4245dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639070 | |||||||
| chr3:134639070 | G | GTT | 78 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(75): Show |
88 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.262+4244_262+4245d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639070 | |||||||
| chr3:134639202 | T | C | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262+4114A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639202 | |||||||
| chr3:134639227 | G | A | 2 | a0001c0003t0002g0211 a0001c0003t0002g0215 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.262+4089C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639227 | |||||||
| chr3:134639267 | C | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+4049G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639267 | |||||||
| chr3:134639267 | C | G | 90 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(87): Show |
103 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.262+4049G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639267 | |||||||
| chr3:134639321 | C | T | 1 | a0001c0003t0002g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.262+3995G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639321 | |||||||
| chr3:134639789 | C | T | 3 | a0001c0001t0008g0054 a0001c0001t0008g0055 a0001c0001t0008g0175 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.262+3527G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639789 | |||||||
| chr3:134639949 | C | CA | 16 | a0001c0001t0014g0052 a0001c0002t0002g0051 a0001c0002t0002g0090 others(13): Show |
16 | HG01175.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.262+3366dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | |||||||
| chr3:134639949 | CA | C | 14 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0193 others(11): Show |
15 | HG01123.hp2 HG02258.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.262+3366delT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | |||||||
| chr3:134639949 | CAA | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0030 others(45): Show |
59 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.262+3365_262+3366d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | |||||||
| chr3:134639949 | CAAA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.262+3364_262+3366d others(5): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | |||||||
| chr3:134640105 | C | T | 80 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(77): Show |
90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.262+3211G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640105 | |||||||
| chr3:134640306 | C | T | 1 | a0001c0003t0002g0219 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262+3010G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640306 | |||||||
| chr3:134640523 | A | G | 1 | a0001c0001t0005g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.262+2793T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640523 | |||||||
| chr3:134640553 | C | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+2763G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640553 | |||||||
| chr3:134640622 | G | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+2694C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640622 | |||||||
| chr3:134641029 | C | T | 7 | a0001c0002t0002g0012 a0001c0002t0002g0037 a0001c0002t0002g0057 others(4): Show |
8 | HG00738.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+2287G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641029 | |||||||
| chr3:134641083 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG00741.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+2233G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641083 | |||||||
| chr3:134641318 | T | C | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+1998A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641318 | |||||||
| chr3:134641570 | G | A | 1 | a0001c0006t0026g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.262+1746C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641570 | |||||||
| chr3:134641683 | T | C | 1 | a0001c0005t0007g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.262+1633A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641683 | |||||||
| chr3:134641712 | C | T | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.262+1604G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641712 | |||||||
| chr3:134641736 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.262+1580G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641736 | |||||||
| chr3:134641737 | G | A | 26 | a0001c0002t0002g0107 a0001c0003t0002g0007 a0001c0003t0002g0027 others(23): Show |
30 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.262+1579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641737 | |||||||
| chr3:134641791 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG00741.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+1525G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641791 | |||||||
| chr3:134641866 | G | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+1450C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641866 | |||||||
| chr3:134641994 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.262+1322T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641994 | |||||||
| chr3:134642187 | G | T | 3 | a0001c0002t0002g0029 a0001c0007t0010g0015 a0001c0007t0010g0083 |
4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1129C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642187 | |||||||
| chr3:134642228 | C | A | 29 | a0001c0002t0002g0107 a0001c0003t0002g0007 a0001c0003t0002g0027 others(26): Show |
35 | HG01069.hp1 HG01099.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.262+1088G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642228 | |||||||
| chr3:134642536 | T | TAG | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.262+778_262+779dup others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642536 | |||||||
| chr3:134642886 | A | G | 1 | a0001c0002t0004g0004 | 4 | NA18981.hp1 NA18982.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+430T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642886 | |||||||
| chr3:134643003 | ATAGT | A | 3 | a0001c0003t0002g0231 a0001c0003t0002g0232 a0001c0003t0002g0233 |
3 | NA18956.hp1 NA18989.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.262+309_262+312del others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134643003 | |||||||
| chr3:134643485 | G | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0099 a0001c0001t0001g0161 others(1): Show |
5 | HG02074.hp2 HG02273.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-107C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643485 | |||||||
| chr3:134643491 | C | T | 1 | a0001c0006t0026g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.200-113G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643491 | |||||||
| chr3:134643559 | G | A | 1 | a0001c0002t0002g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.200-181C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643559 | |||||||
| chr3:134643805 | G | C | 1 | a0001c0002t0002g0164 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.200-427C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643805 | |||||||
| chr3:134643829 | C | CT | 39 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0030 others(36): Show |
48 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.200-452dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | |||||||
| chr3:134643829 | C | CTT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.200-453_200-452dup others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | |||||||
| chr3:134643829 | C | CTTT | 5 | a0001c0001t0008g0175 a0001c0002t0002g0172 a0001c0004t0001g0173 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-454_200-452dup others(3): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | |||||||
| chr3:134643870 | A | C | 1 | a0001c0002t0018g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.200-492T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643870 | |||||||
| chr3:134643888 | G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.200-510C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643888 | |||||||
| chr3:134643946 | C | T | 2 | a0001c0005t0006g0104 a0001c0005t0006g0105 |
2 | NA18951.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.200-568G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643946 | |||||||
| chr3:134643957 | G | A | 13 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643957 | |||||||
| chr3:134644016 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.200-638C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644016 | |||||||
| chr3:134644019 | G | T | 1 | a0001c0005t0006g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.200-641C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644019 | |||||||
| chr3:134644072 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.200-694C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644072 | |||||||
| chr3:134644125 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.200-747C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644125 | |||||||
| chr3:134644152 | C | CAGG | 3 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0101 |
4 | HG00099.hp2 HG00323.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-777_200-775dup others(3): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644152 | |||||||
| chr3:134644364 | G | A | 33 | a0001c0001t0001g0032 a0001c0003t0002g0007 a0001c0003t0002g0027 others(30): Show |
39 | HG00738.hp2 HG01069.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.200-986C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644364 | |||||||
| chr3:134644498 | C | A | 25 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0070 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.200-1120G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644498 | |||||||
| chr3:134644529 | C | T | 1 | a0001c0004t0001g0010 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.200-1151G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644529 | |||||||
| chr3:134644584 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.200-1206G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644584 | |||||||
| chr3:134644750 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.200-1372C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644750 | |||||||
| chr3:134645102 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0089 others(6): Show |
10 | HG01952.hp2 HG01981.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-1724A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645102 | |||||||
| chr3:134645267 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.200-1889G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645267 | |||||||
| chr3:134645268 | G | A | 6 | a0001c0001t0008g0175 a0001c0001t0029g0195 a0001c0002t0002g0172 others(3): Show |
8 | HG01891.hp1 HG02258.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-1890C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645268 | |||||||
| chr3:134645287 | A | G | 33 | a0001c0001t0001g0032 a0001c0003t0002g0007 a0001c0003t0002g0027 others(30): Show |
39 | HG00738.hp2 HG01069.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.200-1909T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645287 | |||||||
| chr3:134645306 | T | C | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.200-1928A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645306 | |||||||
| chr3:134645320 | C | G | 1 | a0001c0004t0001g0009 | 3 | HG03225.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.200-1942G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645320 | |||||||
| chr3:134645549 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+1886G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645549 | |||||||
| chr3:134645789 | G | A | 1 | a0001c0001t0024g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.199+1646C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645789 | |||||||
| chr3:134645988 | G | A | 5 | a0001c0001t0008g0175 a0001c0002t0002g0172 a0001c0004t0001g0173 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+1447C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645988 | |||||||
| chr3:134646047 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0177 others(23): Show |
34 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.199+1388A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646047 | |||||||
| chr3:134646114 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199+1321A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646114 | |||||||
| chr3:134646211 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.199+1224C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646211 | |||||||
| chr3:134646222 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.199+1213A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646222 | |||||||
| chr3:134646289 | C | T | 2 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.199+1146G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646289 | |||||||
| chr3:134646437 | A | G | 1 | a0001c0002t0002g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199+998T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646437 | |||||||
| chr3:134646654 | C | T | 2 | a0001c0007t0010g0015 a0001c0007t0010g0083 |
3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.199+781G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646654 | |||||||
| chr3:134646730 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199+705A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646730 | |||||||
| chr3:134646786 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.199+649C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646786 | |||||||
| chr3:134646911 | C | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.199+524G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646911 | |||||||
| chr3:134647032 | T | C | 2 | a0001c0002t0004g0087 a0001c0002t0015g0088 |
2 | NA18960.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.199+403A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647032 | |||||||
| chr3:134647043 | T | G | 2 | a0001c0005t0006g0199 a0001c0005t0006g0200 |
2 | NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.199+392A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647043 | |||||||
| chr3:134647069 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.199+366G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647069 | |||||||
| chr3:134647173 | C | T | 1 | a0001c0003t0002g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199+262G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647173 | |||||||
| chr3:134647248 | G | A | 1 | a0001c0002t0002g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199+187C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647248 | |||||||
| chr3:134647273 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0092 |
3 | HG01257.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.199+162T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647273 | |||||||
| chr3:134647578 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-81C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647578 | |||||||
| chr3:134647594 | C | T | 1 | a0001c0003t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.137-97G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647594 | |||||||
| chr3:134647611 | CTG | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0026 others(2): Show |
10 | HG01167.hp2 HG01169.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-116_137-115del others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647611 | |||||||
| chr3:134647715 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137-218C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647715 | |||||||
| chr3:134647765 | TTTCCAC | T | 3 | a0001c0002t0002g0029 a0001c0007t0010g0015 a0001c0007t0010g0083 |
4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-274_137-269del others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647765 | |||||||
| chr3:134647920 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137-423T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647920 | |||||||
| chr3:134647959 | C | T | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.137-462G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647959 | |||||||
| chr3:134648083 | C | T | 2 | a0001c0003t0002g0027 a0001c0003t0002g0209 |
3 | HG01168.hp1 HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.137-586G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648083 | |||||||
| chr3:134648084 | G | A | 1 | a0004c0014t0017g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-587C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648084 | |||||||
| chr3:134648114 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137-617G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648114 | |||||||
| chr3:134648209 | C | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0002t0002g0037 others(10): Show |
16 | HG02922.hp2 HG03041.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-712G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648209 | |||||||
| chr3:134648352 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.137-855G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648352 | |||||||
| chr3:134648543 | G | A | 1 | a0005c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.137-1046C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648543 | |||||||
| chr3:134648768 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.137-1271C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648768 | |||||||
| chr3:134648997 | C | T | 2 | a0001c0002t0004g0087 a0001c0002t0015g0088 |
2 | NA18960.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.137-1500G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648997 | |||||||
| chr3:134649130 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1633T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649130 | |||||||
| chr3:134649131 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1634C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649131 | |||||||
| chr3:134649132 | A | ATTCTG | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1636_137-1635i others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649132 | |||||||
| chr3:134649792 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.136+1033T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649792 | |||||||
| chr3:134649972 | C | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+853G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649972 | |||||||
| chr3:134650123 | GGATCCTG others(17): Show |
G | 1 | a0001c0005t0007g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+678_136+701del others(24): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650123 | |||||||
| chr3:134650140 | A | G | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+685T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650140 | |||||||
| chr3:134650219 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.136+606A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650219 | |||||||
| chr3:134650366 | G | T | 2 | a0001c0006t0001g0208 a0001c0006t0026g0207 |
2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.136+459C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650366 | |||||||
| chr3:134650436 | G | A | 1 | a0001c0002t0004g0004 | 4 | NA18981.hp1 NA18982.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+389C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650436 | |||||||
| chr3:134650488 | G | A | 3 | a0001c0002t0002g0029 a0001c0007t0010g0015 a0001c0007t0010g0083 |
4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+337C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650488 | |||||||
| chr3:134650578 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.136+247C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650578 | |||||||
| chr3:134650627 | GCTGCGCG others(11): Show |
G | 1 | a0001c0003t0002g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+180_136+197del others(18): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650627 | |||||||
| chr3:134650722 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136+103T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650722 | |||||||
| chr3:134650779 | G | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+46C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650779 |