Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 401720 |
| ensemblid | ENSG00000261308.4 |
| hgncid | 13287 |
| symbol | FIGNL2 |
| name | fidgetin like 2 |
| refseq_nuc | NM_001384995.1 |
| refseq_prot | NP_001371924.1 |
| ensembl_nuc | ENST00000618634.3 |
| ensembl_prot | ENSP00000491257.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51817899 |
| end | 51848718 |
| strand | - |
| ver | v1.2 |
| region | chr12:51817899-51848718 |
| region5000 | chr12:51812899-51853718 |
| regionname0 | FIGNL2_chr12_51817899_51848718 |
| regionname5000 | FIGNL2_chr12_51812899_51853718 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 653 | 344 | 65 | 58 | 174 | 15 | 31 | 128 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0002 | 1/0 | 653 | 45 | 15 | 10 | 2 | 1 | 16 | 2 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0003 | 0/0 | 653 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0004 | 0/0 | 653 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0005 | 0/0 | 653 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0006 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0007 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0008 | 0/0 | 653 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0009 | 0/0 | 653 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0010 | 0/0 | 653 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0011 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| a0012 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | MHWTP others(648): Show |
chr12 | 51812899 | 51853718 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1959 | 301 | 42 | 55 | 169 | 15 | 19 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0003 | 0/0 | 1959 | 26 | 10 | 3 | 1 | 0 | 12 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0004 | 0/0 | 1959 | 7 | 7 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0007 | 0/0 | 1959 | 4 | 4 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0009 | 0/0 | 1959 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0018 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0019 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0020 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0001c0022 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0002c0002 | 1/0 | 1959 | 43 | 14 | 10 | 2 | 1 | 15 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0002c0014 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0002c0015 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0003c0006 | 0/0 | 1959 | 5 | 5 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0004c0005 | 0/0 | 1959 | 5 | 5 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0005c0008 | 0/0 | 1959 | 2 | 0 | 0 | 0 | 2 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0006c0010 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0007c0021 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0008c0017 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0009c0011 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0010c0012 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0011c0016 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 | ||
| a0012c0013 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | ATGCA others(1954): Show |
chr12 | 51812899 | 51853718 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4705 | 111 | 13 | 9 | 79 | 2 | 8 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0002 | 0/1 | 4705 | 115 | 7 | 25 | 68 | 9 | 5 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0003 | 0/0 | 4705 | 52 | 14 | 15 | 15 | 4 | 4 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0009 | 0/0 | 4705 | 4 | 0 | 0 | 4 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0010 | 0/0 | 4705 | 3 | 3 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0011 | 0/0 | 4705 | 3 | 0 | 2 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0013 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0015 | 0/0 | 4705 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0018 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0019 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0021 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0022 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0023 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0024 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0026 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0027 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0028 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0001t0030 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0003t0001 | 0/0 | 4705 | 19 | 4 | 2 | 1 | 0 | 12 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0003t0006 | 0/0 | 4705 | 6 | 5 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0003t0020 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0004t0005 | 0/0 | 4705 | 7 | 7 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0007t0003 | 0/0 | 4705 | 4 | 4 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0009t0001 | 0/0 | 4705 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0018t0001 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0019t0029 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0020t0017 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0001c0022t0001 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0002c0002t0004 | 1/0 | 4705 | 40 | 11 | 10 | 2 | 1 | 15 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0002c0002t0014 | 0/0 | 4705 | 2 | 2 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0002c0002t0016 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0002c0014t0004 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0002c0015t0004 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0003c0006t0008 | 0/0 | 4705 | 5 | 5 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0004c0005t0007 | 0/0 | 4705 | 5 | 5 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0005c0008t0012 | 0/0 | 4705 | 2 | 0 | 0 | 0 | 2 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0006c0010t0025 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0007c0021t0002 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0008c0017t0013 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0009c0011t0004 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0010c0012t0005 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0011c0016t0002 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| a0012c0013t0001 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | AGTCC others(4700): Show |
chr12 | 51812899 | 51853718 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0009 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0010g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0011g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0013g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0015g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0018g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0019g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0021g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0022g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0023g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0024g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0026g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0027g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0028g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0001t0030g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0006g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0003t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0004t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0007t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0007t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0009t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0018t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0019t0029g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0020t0017g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0001c0022t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0014g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0002t0016g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0014t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0002c0015t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0003c0006t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0003c0006t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0003c0006t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0003c0006t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0004c0005t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0004c0005t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0004c0005t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0004c0005t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0004c0005t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0005c0008t0012g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0005c0008t0012g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0006c0010t0025g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0007c0021t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0008c0017t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0009c0011t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0010c0012t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0011c0016t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| a0012c0013t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | GBR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00280 | hp2 | a0002 | c0002 | t0004 | g0233 | EUR | FIN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0068 | EUR | FIN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00408 | hp2 | a0006 | c0010 | t0025 | g0259 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0065 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00621 | hp1 | a0001 | c0001 | t0022 | g0091 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00639 | hp1 | a0002 | c0002 | t0004 | g0025 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00733 | hp2 | a0002 | c0002 | t0004 | g0119 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00735 | hp1 | a0002 | c0002 | t0004 | g0025 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01070 | hp1 | a0001 | c0003 | t0006 | g0005 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01070 | hp2 | a0001 | c0001 | t0015 | g0026 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01071 | hp1 | a0001 | c0001 | t0015 | g0026 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01099 | hp2 | a0002 | c0002 | t0004 | g0228 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0320 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01167 | hp1 | a0002 | c0002 | t0004 | g0021 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01168 | hp2 | a0002 | c0002 | t0004 | g0011 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01169 | hp2 | a0002 | c0002 | t0004 | g0021 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01192 | hp1 | a0001 | c0001 | t0023 | g0134 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0136 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0046 | AMR | PUR | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0149 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0311 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01433 | hp1 | a0001 | c0001 | t0028 | g0063 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01433 | hp2 | a0002 | c0002 | t0004 | g0011 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01496 | hp2 | a0002 | c0002 | t0004 | g0236 | AMR | CLM | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01516 | hp2 | a0005 | c0008 | t0012 | g0170 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01517 | hp1 | a0005 | c0008 | t0012 | g0157 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0123 | EUR | IBS | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0185 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01891 | hp2 | a0001 | c0004 | t0005 | g0139 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0104 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02055 | hp2 | a0002 | c0002 | t0014 | g0277 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02132 | hp1 | a0007 | c0021 | t0002 | g0087 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02145 | hp1 | a0004 | c0005 | t0007 | g0310 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CDX | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | CDX | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0315 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02257 | hp2 | a0001 | c0004 | t0005 | g0122 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02258 | hp1 | a0001 | c0001 | t0024 | g0179 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02258 | hp2 | a0001 | c0007 | t0003 | g0010 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02280 | hp1 | a0001 | c0007 | t0003 | g0273 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02451 | hp2 | a0001 | c0003 | t0006 | g0005 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0140 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0301 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02615 | hp2 | a0004 | c0005 | t0007 | g0308 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0005 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02630 | hp1 | a0004 | c0005 | t0007 | g0307 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02630 | hp2 | a0003 | c0006 | t0008 | g0045 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02647 | hp1 | a0002 | c0002 | t0014 | g0234 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0235 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02683 | hp2 | a0001 | c0001 | t0011 | g0046 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0077 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02723 | hp1 | a0001 | c0001 | t0030 | g0321 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02723 | hp2 | a0003 | c0006 | t0008 | g0045 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0281 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02818 | hp1 | a0001 | c0003 | t0006 | g0137 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02886 | hp1 | a0001 | c0020 | t0017 | g0048 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02896 | hp1 | a0003 | c0006 | t0008 | g0305 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02897 | hp2 | a0003 | c0006 | t0008 | g0303 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02970 | hp2 | a0008 | c0017 | t0013 | g0182 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0322 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0059 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03041 | hp2 | a0001 | c0003 | t0006 | g0005 | AFR | GWD | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03098 | hp1 | a0001 | c0004 | t0005 | g0187 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0288 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03130 | hp1 | a0001 | c0004 | t0005 | g0291 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0044 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0079 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03195 | hp2 | a0004 | c0005 | t0007 | g0323 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03225 | hp1 | a0001 | c0004 | t0005 | g0324 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0302 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0286 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03453 | hp2 | a0001 | c0001 | t0026 | g0178 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0184 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03486 | hp2 | a0001 | c0004 | t0005 | g0295 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0017 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0042 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03491 | hp2 | a0002 | c0002 | t0004 | g0043 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0017 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0042 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03516 | hp1 | a0002 | c0002 | t0016 | g0050 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03516 | hp2 | a0004 | c0005 | t0007 | g0189 | AFR | ESN | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0106 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0326 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0011 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03688 | hp1 | a0002 | c0002 | t0004 | g0283 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0082 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03704 | hp1 | a0002 | c0015 | t0004 | g0060 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03704 | hp2 | a0002 | c0002 | t0004 | g0056 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03710 | hp1 | a0002 | c0002 | t0004 | g0043 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0290 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0298 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03834 | hp2 | a0009 | c0011 | t0004 | g0078 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03927 | hp1 | a0002 | c0002 | t0004 | g0113 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0279 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04115 | hp1 | a0002 | c0002 | t0004 | g0108 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0237 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0177 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0287 | SAS | BEB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04199 | hp1 | a0002 | c0002 | t0004 | g0072 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0173 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0116 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | STU | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0044 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18522 | hp2 | a0010 | c0012 | t0005 | g0294 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | CHB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18941 | hp1 | a0001 | c0009 | t0001 | g0225 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18950 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18954 | hp1 | a0001 | c0018 | t0001 | g0155 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18957 | hp2 | a0001 | c0001 | t0027 | g0195 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18965 | hp2 | a0011 | c0016 | t0002 | g0202 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18991 | hp1 | a0001 | c0001 | t0021 | g0158 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA18999 | hp2 | a0001 | c0022 | t0001 | g0284 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19030 | hp2 | a0001 | c0004 | t0005 | g0239 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0209 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19043 | hp2 | a0001 | c0003 | t0020 | g0280 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19055 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19056 | hp1 | a0001 | c0009 | t0001 | g0248 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19063 | hp1 | a0001 | c0001 | t0009 | g0066 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19084 | hp2 | a0012 | c0013 | t0001 | g0093 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0289 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0095 | AFR | YRI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | TSI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | TSI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20905 | hp1 | a0001 | c0001 | t0019 | g0080 | SAS | GIH | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | GIH | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02109 | hp1 | a0003 | c0006 | t0008 | g0186 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02109 | hp2 | a0001 | c0019 | t0029 | g0206 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02486 | hp2 | a0001 | c0007 | t0003 | g0010 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0097 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG02559 | hp2 | a0001 | c0007 | t0003 | g0010 | AFR | ACB | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03471 | hp1 | a0002 | c0014 | t0004 | g0304 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | USA | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | USA | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0250 | REF | REF | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0293 | REF | REF | FIGNL2_chr12_51812899_51853718 | FIGNL2 | chr12 | 51812899 | 51853718 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51820981 | G | T | 1 | a0004 | 5 | HG02145.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.1433C>A | p.Ala478Glu | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1623/4705 | 1433/1962 | 478/653 | chr12 | 51820981 | |||
| chr12:51821159 | G | T | 1 | a0008 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1255C>A | p.Pro419Thr | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1445/4705 | 1255/1962 | 419/653 | chr12 | 51821159 | |||
| chr12:51821162 | A | C | 1 | a0011 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.1252T>G | p.Tyr418Asp | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1442/4705 | 1252/1962 | 418/653 | chr12 | 51821162 | |||
| chr12:51821261 | A | C | 1 | a0005 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.1153T>G | p.Cys385Gly | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1343/4705 | 1153/1962 | 385/653 | chr12 | 51821261 | |||
| chr12:51821318 | T | G | 10 | a0001 a0003 a0004 others(7): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
missense_variant | MODERATE | c.1096A>C | p.Thr366Pro | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1286/4705 | 1096/1962 | 366/653 | chr12 | 51821318 | |||
| chr12:51821503 | C | T | 1 | a0010 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.911G>A | p.Cys304Tyr | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1101/4705 | 911/1962 | 304/653 | chr12 | 51821503 | |||
| chr12:51821518 | G | C | 1 | a0007 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.896C>G | p.Ala299Gly | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1086/4705 | 896/1962 | 299/653 | chr12 | 51821518 | |||
| chr12:51821591 | C | T | 1 | a0012 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.823G>A | p.Glu275Lys | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1013/4705 | 823/1962 | 275/653 | chr12 | 51821591 | |||
| chr12:51822101 | G | T | 1 | a0009 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.313C>A | p.Pro105Thr | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 503/4705 | 313/1962 | 105/653 | chr12 | 51822101 | |||
| chr12:51822129 | A | C | 1 | a0006 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.285T>G | p.Asp95Glu | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 475/4705 | 285/1962 | 95/653 | chr12 | 51822129 | |||
| chr12:51822178 | G | A | 1 | a0003 | 5 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
missense_variant | MODERATE | c.236C>T | p.Ala79Val | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 426/4705 | 236/1962 | 79/653 | chr12 | 51822178 | |||
| chr12:51822424 | G | A | 1 | a0001 | 1 | HG02723.hp1 | splice_region_variant | LOW | c.-11C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | chr12 | 51822424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51820728 | G | A | 1 | a0001c0007 | 4 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1686C>T | p.Ala562Ala | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1876/4705 | 1686/1962 | 562/653 | chr12 | 51820728 | |||
| chr12:51820914 | C | G | 1 | a0001c0007 | 4 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1500G>C | p.Arg500Arg | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1690/4705 | 1500/1962 | 500/653 | chr12 | 51820914 | |||
| chr12:51820950 | G | A | 1 | a0001c0020 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1464C>T | p.Leu488Leu | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1654/4705 | 1464/1962 | 488/653 | chr12 | 51820950 | |||
| chr12:51821040 | G | A | 1 | a0001c0009 | 2 | NA18941.hp1 NA19056.hp1 |
synonymous_variant | LOW | c.1374C>T | p.Gly458Gly | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1564/4705 | 1374/1962 | 458/653 | chr12 | 51821040 | |||
| chr12:51821058 | C | G | 1 | a0001c0018 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1356G>C | p.Thr452Thr | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1546/4705 | 1356/1962 | 452/653 | chr12 | 51821058 | |||
| chr12:51821088 | G | A | 2 | a0001c0019 a0001c0020 |
2 | HG02109.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.1326C>T | p.Gly442Gly | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1516/4705 | 1326/1962 | 442/653 | chr12 | 51821088 | |||
| chr12:51821151 | G | A | 1 | a0002c0014 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1263C>T | p.Ser421Ser | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1453/4705 | 1263/1962 | 421/653 | chr12 | 51821151 | |||
| chr12:51821163 | G | A | 1 | a0002c0015 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1251C>T | p.Ala417Ala | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1441/4705 | 1251/1962 | 417/653 | chr12 | 51821163 | |||
| chr12:51821421 | C | T | 2 | a0001c0003 a0001c0022 |
27 | HG01070.hp1 HG01109.hp1 HG01346.hp1 others(24): Show |
synonymous_variant | LOW | c.993G>A | p.Lys331Lys | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1183/4705 | 993/1962 | 331/653 | chr12 | 51821421 | |||
| chr12:51821646 | C | T | 1 | a0003c0006 | 5 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.768G>A | p.Ala256Ala | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 958/4705 | 768/1962 | 256/653 | chr12 | 51821646 | |||
| chr12:51821886 | G | C | 1 | a0001c0022 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.528C>G | p.Gly176Gly | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 718/4705 | 528/1962 | 176/653 | chr12 | 51821886 | |||
| chr12:51822027 | C | T | 3 | a0001c0004 a0003c0006 a0010c0012 |
13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
synonymous_variant | LOW | c.387G>A | p.Leu129Leu | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 577/4705 | 387/1962 | 129/653 | chr12 | 51822027 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51817903 | T | C | 1 | a0004c0005t0007 | 5 | HG02145.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2549A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2549 | chr12 | 51817903 | ||||||
| chr12:51818019 | C | T | 2 | a0002c0002t0014 a0002c0002t0016 |
3 | HG02055.hp2 HG02647.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2433G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2433 | chr12 | 51818019 | ||||||
| chr12:51818073 | G | T | 2 | a0001c0001t0024 a0001c0001t0026 |
2 | HG02258.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2379C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2379 | chr12 | 51818073 | ||||||
| chr12:51818087 | A | G | 15 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0019 others(12): Show |
159 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2365T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2365 | chr12 | 51818087 | ||||||
| chr12:51818158 | G | A | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*2294C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2294 | chr12 | 51818158 | ||||||
| chr12:51818343 | A | G | 1 | a0001c0001t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 2109 | chr12 | 51818343 | ||||||
| chr12:51818504 | T | C | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*1948A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1948 | chr12 | 51818504 | ||||||
| chr12:51818543 | G | A | 1 | a0001c0003t0006 | 6 | HG01070.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1909C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1909 | chr12 | 51818543 | ||||||
| chr12:51818545 | G | C | 1 | a0006c0010t0025 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1907 | chr12 | 51818545 | ||||||
| chr12:51818548 | G | A | 1 | a0001c0001t0026 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1904C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1904 | chr12 | 51818548 | ||||||
| chr12:51818560 | C | G | 1 | a0001c0001t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1892 | chr12 | 51818560 | ||||||
| chr12:51818617 | A | G | 17 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0018 others(14): Show |
163 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1835T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1835 | chr12 | 51818617 | ||||||
| chr12:51818644 | G | C | 7 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0022 others(4): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1808 | chr12 | 51818644 | ||||||
| chr12:51818705 | A | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*1747T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1747 | chr12 | 51818705 | ||||||
| chr12:51818728 | T | G | 1 | a0001c0001t0028 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1724 | chr12 | 51818728 | ||||||
| chr12:51819203 | T | G | 1 | a0001c0001t0019 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1249 | chr12 | 51819203 | ||||||
| chr12:51819285 | A | C | 1 | a0003c0006t0008 | 5 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1167T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 1167 | chr12 | 51819285 | ||||||
| chr12:51819457 | T | C | 3 | a0001c0004t0005 a0003c0006t0008 a0010c0012t0005 |
13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*995A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 995 | chr12 | 51819457 | ||||||
| chr12:51819617 | C | G | 1 | a0001c0001t0022 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 835 | chr12 | 51819617 | ||||||
| chr12:51819637 | A | G | 2 | a0001c0019t0029 a0001c0020t0017 |
2 | HG02109.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 815 | chr12 | 51819637 | ||||||
| chr12:51819674 | T | G | 1 | a0001c0003t0020 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 778 | chr12 | 51819674 | ||||||
| chr12:51819793 | T | G | 1 | a0001c0001t0021 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 659 | chr12 | 51819793 | ||||||
| chr12:51819855 | T | C | 1 | a0001c0001t0015 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*597A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 597 | chr12 | 51819855 | ||||||
| chr12:51820030 | C | T | 15 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0019 others(12): Show |
163 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*422G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 422 | chr12 | 51820030 | ||||||
| chr12:51820355 | C | A | 2 | a0001c0019t0029 a0001c0020t0017 |
2 | HG02109.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*97G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 2/2 | 97 | chr12 | 51820355 | ||||||
| chr12:51848603 | C | G | 3 | a0001c0001t0010 a0001c0020t0017 a0002c0002t0016 |
5 | HG02622.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-75G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/2 | 26190 | chr12 | 51848603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51822636 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-11-212G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822636 | |||||||
| chr12:51822733 | C | A | 1 | a0001c0001t0001g0297 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-11-309G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822733 | |||||||
| chr12:51822762 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-11-338T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822762 | |||||||
| chr12:51822800 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0030g0321 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-11-376C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822800 | |||||||
| chr12:51822816 | A | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0141 others(3): Show |
7 | HG00423.hp2 HG00597.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-392T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822816 | |||||||
| chr12:51822849 | C | T | 1 | a0002c0002t0004g0326 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11-425G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822849 | |||||||
| chr12:51822957 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-11-533A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51822957 | |||||||
| chr12:51823024 | T | C | 1 | a0001c0001t0013g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-11-600A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823024 | |||||||
| chr12:51823039 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-11-615C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823039 | |||||||
| chr12:51823085 | A | G | 1 | a0008c0017t0013g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11-661T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823085 | |||||||
| chr12:51823113 | G | A | 95 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(92): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11-689C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823113 | |||||||
| chr12:51823219 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0216 |
2 | NA18968.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-11-795T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823219 | |||||||
| chr12:51823260 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-836C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823260 | |||||||
| chr12:51823311 | G | A | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-887C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823311 | |||||||
| chr12:51823431 | T | C | 1 | a0001c0004t0005g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11-1007A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823431 | |||||||
| chr12:51823526 | T | G | 1 | a0003c0006t0008g0045 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-11-1102A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823526 | |||||||
| chr12:51823529 | T | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-1105A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823529 | |||||||
| chr12:51823631 | C | T | 1 | a0001c0020t0017g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-11-1207G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823631 | |||||||
| chr12:51823675 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-11-1251C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823675 | |||||||
| chr12:51823915 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-11-1491G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51823915 | |||||||
| chr12:51824092 | C | T | 47 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(44): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-1668G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824092 | |||||||
| chr12:51824191 | G | C | 1 | a0001c0001t0003g0068 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-11-1767C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824191 | |||||||
| chr12:51824221 | C | T | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-1797G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824221 | |||||||
| chr12:51824226 | T | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-1802A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824226 | |||||||
| chr12:51824267 | CTTTGAAA others(6): Show |
C | 1 | a0001c0001t0002g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-11-1856_-11-1844d others(15): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824267 | |||||||
| chr12:51824296 | G | A | 3 | a0002c0002t0014g0234 a0002c0002t0014g0277 a0002c0002t0016g0050 |
3 | HG02055.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-1872C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824296 | |||||||
| chr12:51824377 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0160 a0001c0001t0021g0158 |
4 | NA18991.hp1 NA19055.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-1953G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824377 | |||||||
| chr12:51824388 | C | T | 1 | a0002c0002t0014g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11-1964G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824388 | |||||||
| chr12:51824490 | A | G | 2 | a0001c0007t0003g0010 a0001c0007t0003g0273 |
4 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2066T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824490 | |||||||
| chr12:51824575 | A | T | 1 | a0001c0001t0002g0047 | 2 | NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-11-2151T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824575 | |||||||
| chr12:51824577 | G | T | 1 | a0008c0017t0013g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11-2153C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824577 | |||||||
| chr12:51824742 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
165 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-11-2318C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824742 | |||||||
| chr12:51824809 | C | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(94): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-11-2385G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824809 | |||||||
| chr12:51824819 | G | A | 1 | a0004c0005t0007g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11-2395C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824819 | |||||||
| chr12:51824863 | G | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
107 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-11-2439C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824863 | |||||||
| chr12:51824870 | A | G | 47 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(44): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-2446T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824870 | |||||||
| chr12:51824904 | C | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
165 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-11-2480G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824904 | |||||||
| chr12:51824913 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-11-2489C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51824913 | |||||||
| chr12:51825111 | G | GT | 126 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
151 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11-2688dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825111 | |||||||
| chr12:51825111 | GT | G | 6 | a0001c0001t0001g0124 a0001c0001t0001g0183 a0001c0001t0018g0095 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-2688delA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825111 | |||||||
| chr12:51825152 | A | G | 3 | a0001c0003t0001g0282 a0001c0003t0001g0286 a0001c0003t0001g0287 |
3 | HG03239.hp1 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-11-2728T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825152 | |||||||
| chr12:51825294 | G | C | 47 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(44): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-2870C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825294 | |||||||
| chr12:51825358 | T | C | 48 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(45): Show |
59 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-2934A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825358 | |||||||
| chr12:51825435 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11-3011G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825435 | |||||||
| chr12:51825540 | T | C | 1 | a0002c0002t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11-3116A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825540 | |||||||
| chr12:51825553 | A | T | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-3129T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825553 | |||||||
| chr12:51825584 | C | T | 28 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0024 others(25): Show |
36 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.-11-3160G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825584 | |||||||
| chr12:51825603 | A | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-3179T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825603 | |||||||
| chr12:51825619 | C | CT | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(95): Show |
119 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-3196dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825619 | |||||||
| chr12:51825619 | C | CTT | 47 | a0001c0001t0001g0143 a0001c0001t0003g0009 a0001c0001t0003g0012 others(44): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.-11-3197_-11-3196d others(4): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825619 | |||||||
| chr12:51825647 | C | T | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-3223G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825647 | |||||||
| chr12:51825656 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0156 a0001c0001t0001g0172 others(6): Show |
10 | HG01981.hp1 HG01993.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-3232C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825656 | |||||||
| chr12:51825686 | G | T | 1 | a0001c0003t0001g0311 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-11-3262C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825686 | |||||||
| chr12:51825696 | A | G | 3 | a0001c0003t0006g0005 a0001c0003t0006g0137 a0001c0003t0006g0140 |
6 | HG01070.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-3272T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51825696 | |||||||
| chr12:51826035 | T | C | 22 | a0001c0003t0001g0042 a0001c0003t0001g0054 a0001c0003t0001g0082 others(19): Show |
26 | HG01070.hp1 HG01109.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.-11-3611A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826035 | |||||||
| chr12:51826098 | C | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(94): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-11-3674G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826098 | |||||||
| chr12:51826171 | GC | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(283): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-11-3748delG | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826171 | |||||||
| chr12:51826177 | C | G | 1 | a0001c0001t0003g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-11-3753G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826177 | |||||||
| chr12:51826185 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-11-3761C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826185 | |||||||
| chr12:51826348 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-3924C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826348 | |||||||
| chr12:51826367 | G | A | 2 | a0001c0019t0029g0206 a0001c0020t0017g0048 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-11-3943C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826367 | |||||||
| chr12:51826400 | G | A | 2 | a0005c0008t0012g0157 a0005c0008t0012g0170 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-11-3976C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826400 | |||||||
| chr12:51826453 | A | G | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4029T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826453 | |||||||
| chr12:51826473 | C | CA | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
108 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-11-4050dupT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826473 | |||||||
| chr12:51826473 | C | CAA | 6 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0230 others(3): Show |
6 | NA18940.hp1 NA18953.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-4051_-11-4050d others(4): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826473 | |||||||
| chr12:51826473 | CA | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(83): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-11-4050delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826473 | |||||||
| chr12:51826495 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-11-4071G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826495 | |||||||
| chr12:51826499 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(87): Show |
110 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-11-4075G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826499 | |||||||
| chr12:51826617 | C | T | 1 | a0001c0003t0001g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-11-4193G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826617 | |||||||
| chr12:51826627 | G | A | 1 | a0001c0001t0013g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-11-4203C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826627 | |||||||
| chr12:51826632 | TC | T | 48 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(45): Show |
59 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-4209delG | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826632 | |||||||
| chr12:51826640 | C | CA | 10 | a0002c0002t0004g0017 a0002c0002t0004g0106 a0002c0002t0004g0108 others(7): Show |
11 | HG01255.hp2 HG02055.hp2 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-4217dupT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826640 | |||||||
| chr12:51826640 | CA | C | 23 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0103 others(20): Show |
25 | HG00438.hp1 HG00609.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-4217delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826640 | |||||||
| chr12:51826640 | CAA | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(155): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.-11-4218_-11-4217d others(4): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826640 | |||||||
| chr12:51826640 | CAAA | C | 18 | a0001c0001t0002g0070 a0001c0001t0002g0096 a0001c0001t0002g0098 others(15): Show |
19 | HG00438.hp2 HG01516.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.-11-4219_-11-4217d others(5): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826640 | |||||||
| chr12:51826640 | CAAAA | C | 85 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(82): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-11-4220_-11-4217d others(6): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826640 | |||||||
| chr12:51826761 | G | A | 1 | a0001c0001t0003g0309 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11-4337C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826761 | |||||||
| chr12:51826862 | TCACGTGA others(17): Show |
T | 1 | a0001c0001t0003g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11-4462_-11-4439d others(26): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826862 | |||||||
| chr12:51826879 | C | T | 1 | a0001c0001t0013g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-11-4455G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826879 | |||||||
| chr12:51826940 | A | G | 1 | a0001c0004t0005g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11-4516T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51826940 | |||||||
| chr12:51827055 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-11-4631T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827055 | |||||||
| chr12:51827118 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0034 others(20): Show |
37 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.-11-4694G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827118 | |||||||
| chr12:51827184 | C | T | 44 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0019 others(41): Show |
54 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11-4760G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827184 | |||||||
| chr12:51827390 | G | GT | 5 | a0001c0001t0001g0176 a0001c0001t0002g0003 a0001c0001t0002g0023 others(2): Show |
9 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-4967dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827390 | |||||||
| chr12:51827404 | T | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4980A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827404 | |||||||
| chr12:51827631 | C | G | 1 | a0001c0001t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-5207G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827631 | |||||||
| chr12:51827726 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11-5302T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827726 | |||||||
| chr12:51827771 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-5347C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827771 | |||||||
| chr12:51827821 | C | T | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-5397G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827821 | |||||||
| chr12:51827841 | G | C | 1 | a0001c0001t0002g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-11-5417C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827841 | |||||||
| chr12:51827843 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0296 |
3 | HG01891.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-11-5419G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827843 | |||||||
| chr12:51827844 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-11-5420C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827844 | |||||||
| chr12:51827956 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-11-5532C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827956 | |||||||
| chr12:51827999 | T | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-11-5575A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51827999 | |||||||
| chr12:51828175 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-11-5751G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51828175 | |||||||
| chr12:51828750 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-11-6326T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51828750 | |||||||
| chr12:51828836 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0299 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-11-6412G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51828836 | |||||||
| chr12:51829023 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-6599T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829023 | |||||||
| chr12:51829273 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-6849C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829273 | |||||||
| chr12:51829299 | G | A | 22 | a0001c0003t0001g0042 a0001c0003t0001g0054 a0001c0003t0001g0082 others(19): Show |
26 | HG01070.hp1 HG01109.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.-11-6875C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829299 | |||||||
| chr12:51829634 | T | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG02615.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-7210A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829634 | |||||||
| chr12:51829810 | AAAGG | A | 14 | a0001c0001t0001g0027 a0001c0001t0001g0074 a0001c0001t0001g0124 others(11): Show |
15 | HG01346.hp1 HG02451.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-7390_-11-7387d others(6): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829810 | |||||||
| chr12:51829859 | A | C | 1 | a0001c0003t0001g0298 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-11-7435T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51829859 | |||||||
| chr12:51830007 | G | T | 92 | a0001c0001t0001g0256 a0001c0001t0002g0001 a0001c0001t0002g0002 others(89): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-11-7583C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830007 | |||||||
| chr12:51830145 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11-7721G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830145 | |||||||
| chr12:51830294 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02040.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-11-7870T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830294 | |||||||
| chr12:51830370 | T | C | 98 | a0001c0001t0001g0256 a0001c0001t0002g0001 a0001c0001t0002g0002 others(95): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11-7946A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830370 | |||||||
| chr12:51830377 | A | G | 1 | a0008c0017t0013g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11-7953T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830377 | |||||||
| chr12:51830492 | TG | T | 39 | a0001c0001t0002g0007 a0001c0001t0002g0232 a0001c0001t0002g0238 others(36): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11-8069delC | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830492 | |||||||
| chr12:51830493 | G | GT | 53 | a0001c0001t0001g0192 a0001c0001t0001g0229 a0001c0001t0001g0256 others(50): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11-8070dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830493 | |||||||
| chr12:51830493 | G | T | 2 | a0001c0001t0002g0007 a0001c0001t0003g0073 |
2 | HG01952.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-11-8069C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830493 | |||||||
| chr12:51830531 | G | A | 1 | a0001c0003t0001g0042 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-11-8107C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830531 | |||||||
| chr12:51830537 | G | C | 2 | a0001c0004t0005g0139 a0001c0004t0005g0187 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-11-8113C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830537 | |||||||
| chr12:51830632 | C | T | 1 | a0002c0002t0004g0228 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-11-8208G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830632 | |||||||
| chr12:51830646 | T | C | 1 | a0001c0003t0020g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11-8222A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830646 | |||||||
| chr12:51830681 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0103 a0001c0001t0001g0110 |
3 | NA18977.hp2 NA19012.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-11-8257A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830681 | |||||||
| chr12:51830685 | G | A | 1 | a0002c0014t0004g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11-8261C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830685 | |||||||
| chr12:51830690 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-8266T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830690 | |||||||
| chr12:51830713 | A | C | 27 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0090 others(24): Show |
31 | HG01516.hp1 HG01884.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11-8289T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830713 | |||||||
| chr12:51830713 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0162 |
2 | NA18970.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-11-8289T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830713 | |||||||
| chr12:51830720 | T | A | 1 | a0001c0001t0002g0221 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-11-8296A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830720 | |||||||
| chr12:51830731 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-11-8307A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830731 | |||||||
| chr12:51830732 | T | C | 1 | a0002c0002t0004g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-8308A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830732 | |||||||
| chr12:51830750 | T | C | 294 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(291): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-11-8326A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830750 | |||||||
| chr12:51830770 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0154 a0001c0001t0001g0204 others(6): Show |
10 | HG02970.hp1 NA18947.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-8346T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830770 | |||||||
| chr12:51830770 | A | T | 1 | a0001c0001t0013g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-11-8346T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830770 | |||||||
| chr12:51830774 | G | A | 1 | a0001c0003t0001g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-11-8350C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830774 | |||||||
| chr12:51830776 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0265 |
2 | NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-11-8352G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830776 | |||||||
| chr12:51830780 | A | G | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0003t0001g0286 others(1): Show |
4 | HG01358.hp2 HG03017.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-8356T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830780 | |||||||
| chr12:51830785 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11-8361G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51830785 | |||||||
| chr12:51831079 | A | G | 22 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0090 others(19): Show |
25 | HG00621.hp2 HG01884.hp2 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-8655T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831079 | |||||||
| chr12:51831189 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0100 a0001c0001t0001g0101 others(42): Show |
59 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-8765A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831189 | |||||||
| chr12:51831254 | G | A | 1 | a0001c0001t0003g0309 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11-8830C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831254 | |||||||
| chr12:51831265 | C | T | 1 | a0004c0005t0007g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11-8841G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831265 | |||||||
| chr12:51831479 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-11-9055C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831479 | |||||||
| chr12:51831573 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-11-9149G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831573 | |||||||
| chr12:51831576 | T | G | 1 | a0001c0003t0001g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-11-9152A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831576 | |||||||
| chr12:51831709 | A | C | 1 | a0001c0003t0001g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-11-9285T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831709 | |||||||
| chr12:51831840 | A | G | 3 | a0001c0001t0030g0321 a0001c0004t0005g0187 a0001c0004t0005g0324 |
3 | HG02723.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-11-9416T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831840 | |||||||
| chr12:51831842 | A | T | 2 | a0001c0001t0002g0210 a0001c0001t0002g0243 |
2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-11-9418T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831842 | |||||||
| chr12:51831854 | T | A | 106 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0124 others(103): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-11-9430A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51831854 | |||||||
| chr12:51832005 | A | C | 8 | a0002c0014t0004g0304 a0003c0006t0008g0045 a0003c0006t0008g0186 others(5): Show |
9 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-9581T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832005 | |||||||
| chr12:51832159 | A | G | 4 | a0001c0004t0005g0122 a0001c0004t0005g0291 a0001c0004t0005g0295 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9735T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832159 | |||||||
| chr12:51832312 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-11-9888G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832312 | |||||||
| chr12:51832618 | G | A | 1 | a0001c0003t0006g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-10194C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832618 | |||||||
| chr12:51832693 | A | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0100 others(49): Show |
67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-11-10269T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832693 | |||||||
| chr12:51832816 | A | G | 8 | a0001c0001t0001g0124 a0001c0001t0001g0183 a0001c0001t0003g0315 others(5): Show |
9 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-10392T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832816 | |||||||
| chr12:51832982 | C | G | 1 | a0001c0003t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11-10558G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51832982 | |||||||
| chr12:51833045 | C | CT | 4 | a0001c0001t0003g0040 a0001c0001t0003g0278 a0001c0001t0003g0325 others(1): Show |
5 | HG02055.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-10622dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833045 | |||||||
| chr12:51833047 | T | C | 2 | a0001c0001t0003g0180 a0001c0001t0003g0306 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-11-10623A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833047 | |||||||
| chr12:51833105 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-10681G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833105 | |||||||
| chr12:51833128 | G | T | 5 | a0001c0004t0005g0122 a0001c0004t0005g0291 a0001c0004t0005g0295 others(2): Show |
5 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-10704C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833128 | |||||||
| chr12:51833155 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0027 others(70): Show |
85 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-11-10731G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833155 | |||||||
| chr12:51833294 | G | T | 9 | a0001c0001t0001g0074 a0001c0001t0001g0300 a0001c0001t0001g0316 others(6): Show |
9 | HG02257.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-10870C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833294 | |||||||
| chr12:51833373 | C | G | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11-10949G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833373 | |||||||
| chr12:51833445 | T | C | 1 | a0001c0003t0001g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-11-11021A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833445 | |||||||
| chr12:51833481 | C | T | 1 | a0001c0001t0011g0046 | 2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-11-11057G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833481 | |||||||
| chr12:51833531 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11-11107G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833531 | |||||||
| chr12:51833616 | G | C | 1 | a0001c0001t0003g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-11-11192C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833616 | |||||||
| chr12:51833617 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-11-11193G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833617 | |||||||
| chr12:51833620 | C | T | 1 | a0001c0003t0020g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11-11196G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833620 | |||||||
| chr12:51833689 | G | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0100 others(63): Show |
84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-11-11265C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833689 | |||||||
| chr12:51833714 | C | T | 118 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(115): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11-11290G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833714 | |||||||
| chr12:51833803 | G | A | 3 | a0001c0001t0003g0099 a0001c0001t0030g0321 a0001c0004t0005g0324 |
3 | HG02723.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-11-11379C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833803 | |||||||
| chr12:51833891 | C | T | 1 | a0001c0001t0028g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11-11467G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833891 | |||||||
| chr12:51833950 | C | CGGACGGA others(57): Show |
3 | a0001c0003t0001g0207 a0001c0004t0005g0295 a0010c0012t0005g0294 |
3 | HG03486.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-11-11590_-11-1152 others(68): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51833950 | |||||||
| chr12:51834000 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11576T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834000 | |||||||
| chr12:51834000 | AATGGACA others(25): Show |
A | 2 | a0001c0001t0030g0321 a0001c0004t0005g0324 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-11-11608_-11-1157 others(36): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834000 | |||||||
| chr12:51834006 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11582G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834006 | |||||||
| chr12:51834007 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11583T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834007 | |||||||
| chr12:51834010 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11586G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834010 | |||||||
| chr12:51834011 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11587T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834011 | |||||||
| chr12:51834012 | A | AATGGATG others(169): Show |
2 | a0001c0001t0002g0203 a0011c0016t0002g0202 |
2 | NA18965.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-11-11589_-11-1158 others(180): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834012 | |||||||
| chr12:51834015 | G | GGACAGAT others(29): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11592_-11-1159 others(40): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834015 | |||||||
| chr12:51834018 | C | CGGATGGA others(125): Show |
1 | a0001c0001t0001g0100 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-11-11595_-11-1159 others(136): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834018 | C | CGGATGGA others(69): Show |
11 | a0001c0001t0001g0191 a0001c0001t0003g0125 a0001c0001t0003g0138 others(8): Show |
14 | HG00738.hp2 HG01070.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11-11595_-11-1159 others(80): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834018 | C | CGGATGGA others(61): Show |
55 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0101 others(52): Show |
73 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-11595_-11-1159 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834018 | C | CGGATGGA others(73): Show |
6 | a0001c0001t0001g0074 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02257.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-11595_-11-1159 others(84): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834018 | C | CGGATGGG others(61): Show |
1 | a0001c0001t0003g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-11-11595_-11-1159 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834018 | C | T | 102 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(99): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11-11594G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834018 | |||||||
| chr12:51834021 | A | ATGGATGG others(61): Show |
1 | a0001c0001t0002g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11-11598_-11-1159 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834021 | |||||||
| chr12:51834021 | A | ATGGATGG others(65): Show |
2 | a0001c0001t0002g0105 a0001c0001t0002g0107 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-11-11598_-11-1159 others(76): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834021 | |||||||
| chr12:51834025 | A | ATGGATGG others(61): Show |
48 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
58 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-11602_-11-1160 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834025 | |||||||
| chr12:51834025 | A | ATGGATGG others(53): Show |
1 | a0001c0001t0001g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-11-11602_-11-1160 others(64): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834025 | |||||||
| chr12:51834025 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0152 |
3 | HG01069.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11-11601T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834025 | |||||||
| chr12:51834032 | G | AATGGATG others(69): Show |
1 | a0001c0003t0020g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11-11608_-11-1160 others(80): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834032 | |||||||
| chr12:51834032 | G | GATGGATG others(97): Show |
1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-11609_-11-1160 others(108): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834032 | |||||||
| chr12:51834038 | TG | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0092 a0001c0001t0001g0215 others(2): Show |
7 | NA18957.hp1 NA18971.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-11615delC | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834038 | |||||||
| chr12:51834044 | A | G | 1 | a0002c0002t0004g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-11-11620T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834044 | |||||||
| chr12:51834078 | TAGAC | T | 8 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0211 others(5): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-11658_-11-1165 others(8): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834078 | |||||||
| chr12:51834082 | C | CAGACAGA others(65): Show |
1 | a0001c0001t0002g0002 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-11-11659_-11-1165 others(76): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(57): Show |
1 | a0001c0001t0002g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-11-11659_-11-1165 others(68): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(61): Show |
1 | a0002c0002t0004g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-11-11659_-11-1165 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(65): Show |
91 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(88): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-11-11659_-11-1165 others(76): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(141): Show |
1 | a0001c0009t0001g0248 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11-11659_-11-1165 others(152): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(69): Show |
2 | a0001c0001t0002g0210 a0001c0001t0002g0243 |
2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-11-11659_-11-1165 others(80): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGACGGA others(85): Show |
2 | a0001c0001t0002g0127 a0001c0003t0001g0282 |
2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-11-11659_-11-1165 others(96): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834082 | C | CAGATGGA others(65): Show |
2 | a0002c0002t0004g0025 a0002c0002t0004g0119 |
3 | HG00639.hp1 HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-11-11659_-11-1165 others(76): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834082 | |||||||
| chr12:51834086 | C | CGGATGGG others(61): Show |
1 | a0001c0001t0003g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11-11663_-11-1166 others(72): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834086 | |||||||
| chr12:51834086 | C | CGGATGGG others(213): Show |
2 | a0001c0003t0001g0042 a0001c0003t0001g0279 |
3 | HG03491.hp1 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-11-11663_-11-1166 others(224): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834086 | |||||||
| chr12:51834086 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-11-11662G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834086 | |||||||
| chr12:51834087 | A | G | 29 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0297 others(26): Show |
31 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-11-11663T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834087 | |||||||
| chr12:51834089 | A | ATGGG | 10 | a0001c0001t0010g0049 a0001c0003t0001g0320 a0002c0002t0004g0237 others(7): Show |
11 | HG01109.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-11666_-11-1166 others(8): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834089 | |||||||
| chr12:51834090 | C | T | 29 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0297 others(26): Show |
31 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-11-11666G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834090 | |||||||
| chr12:51834091 | G | A | 3 | a0001c0001t0003g0241 a0001c0003t0001g0042 a0001c0003t0001g0279 |
4 | HG02886.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11667C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834091 | |||||||
| chr12:51834093 | A | G | 19 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0297 others(16): Show |
20 | HG02055.hp2 HG02572.hp2 HG02818.hp1 others(17): Show |
intron_variant | MODIFIER | c.-11-11669T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834093 | |||||||
| chr12:51834094 | T | C | 3 | a0001c0001t0003g0241 a0001c0003t0001g0042 a0001c0003t0001g0279 |
4 | HG02886.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11670A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834094 | |||||||
| chr12:51834097 | G | A | 32 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0297 others(29): Show |
35 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-11-11673C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834097 | |||||||
| chr12:51834097 | G | GTGGATGG others(1): Show |
5 | a0001c0001t0001g0258 a0001c0001t0002g0071 a0001c0001t0002g0163 others(2): Show |
5 | HG00438.hp2 HG02273.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-11674_-11-1167 others(12): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834097 | |||||||
| chr12:51834101 | A | ATGGT | 68 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(65): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-11-11678_-11-1167 others(8): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834101 | |||||||
| chr12:51834101 | A | G | 3 | a0001c0001t0003g0241 a0001c0003t0001g0042 a0001c0003t0001g0279 |
4 | HG02886.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11677T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834101 | |||||||
| chr12:51834101 | A | T | 4 | a0001c0001t0010g0049 a0001c0003t0001g0320 a0002c0002t0014g0234 others(1): Show |
4 | HG01109.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11677T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834101 | |||||||
| chr12:51834105 | A | ATGGATGA others(53): Show |
2 | a0001c0001t0003g0278 a0002c0002t0014g0277 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-11-11682_-11-1168 others(64): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834105 | |||||||
| chr12:51834105 | A | T | 42 | a0001c0001t0001g0117 a0001c0001t0001g0183 a0001c0001t0001g0263 others(39): Show |
50 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11-11681T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834105 | |||||||
| chr12:51834109 | T | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(125): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-11-11685A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834109 | T | TTGGA | 82 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0088 others(79): Show |
106 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-11-11689_-11-1168 others(8): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834109 | T | TTGGATGG others(1): Show |
62 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(59): Show |
71 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-11693_-11-1168 others(12): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834109 | T | TTGGATGG others(89): Show |
2 | a0001c0003t0001g0286 a0001c0003t0001g0287 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-11-11686_-11-1168 others(100): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834109 | TTGGA | T | 5 | a0001c0001t0001g0300 a0001c0004t0005g0122 a0001c0004t0005g0291 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-11689_-11-1168 others(8): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834109 | TTGGATGG others(1): Show |
T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0325 |
3 | HG03139.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11-11693_-11-1168 others(12): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834109 | |||||||
| chr12:51834113 | A | ATGGATGA others(53): Show |
1 | a0001c0003t0006g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-11-11690_-11-1168 others(64): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834113 | |||||||
| chr12:51834116 | G | A | 5 | a0002c0014t0004g0304 a0003c0006t0008g0045 a0003c0006t0008g0186 others(2): Show |
6 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-11692C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834116 | |||||||
| chr12:51834117 | A | T | 2 | a0001c0001t0003g0278 a0002c0002t0014g0277 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-11-11693T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834117 | |||||||
| chr12:51834141 | A | G | 1 | a0001c0004t0005g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11-11717T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834141 | |||||||
| chr12:51834182 | G | T | 2 | a0001c0001t0003g0125 a0001c0003t0020g0280 |
2 | HG00738.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11-11758C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834182 | |||||||
| chr12:51834253 | T | C | 2 | a0001c0001t0002g0161 a0001c0009t0001g0225 |
2 | NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-11-11829A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834253 | |||||||
| chr12:51834275 | AG | A | 5 | a0001c0001t0001g0300 a0001c0003t0001g0302 a0001c0004t0005g0122 others(2): Show |
5 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-11852delC | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834275 | |||||||
| chr12:51834371 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0003g0133 |
2 | HG01256.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.-11-11947C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834371 | |||||||
| chr12:51834417 | T | C | 1 | a0002c0002t0004g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11-11993A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834417 | |||||||
| chr12:51834426 | T | G | 2 | a0001c0003t0001g0302 a0001c0003t0001g0311 |
2 | HG01346.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-11-12002A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834426 | |||||||
| chr12:51834521 | G | A | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-11-12097C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834521 | |||||||
| chr12:51834696 | G | C | 2 | a0001c0001t0030g0321 a0001c0004t0005g0239 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-11-12272C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834696 | |||||||
| chr12:51834708 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-11-12284G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834708 | |||||||
| chr12:51834777 | G | A | 6 | a0001c0001t0001g0297 a0001c0001t0001g0299 a0001c0001t0003g0180 others(3): Show |
7 | HG01884.hp1 HG03239.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-12353C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834777 | |||||||
| chr12:51834966 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-11-12542C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51834966 | |||||||
| chr12:51835188 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-11-12764C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835188 | |||||||
| chr12:51835265 | C | G | 1 | a0001c0001t0024g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11-12841G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835265 | |||||||
| chr12:51835267 | A | C | 2 | a0001c0001t0010g0015 a0001c0001t0010g0049 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-11-12843T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835267 | |||||||
| chr12:51835282 | C | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0190 a0001c0001t0001g0191 others(4): Show |
8 | HG01981.hp1 HG01993.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-12858G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835282 | |||||||
| chr12:51835365 | C | T | 6 | a0001c0001t0001g0074 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02257.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-12941G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835365 | |||||||
| chr12:51835381 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11-12957G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835381 | |||||||
| chr12:51835395 | G | A | 4 | a0001c0001t0003g0099 a0001c0001t0024g0179 a0001c0001t0026g0178 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-12971C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835395 | |||||||
| chr12:51835481 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11-13057G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835481 | |||||||
| chr12:51835581 | A | T | 10 | a0001c0001t0003g0040 a0001c0001t0003g0180 a0001c0001t0003g0276 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+12959T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835581 | |||||||
| chr12:51835652 | C | CACAACAA others(1): Show |
4 | a0001c0001t0003g0099 a0001c0001t0024g0179 a0001c0001t0026g0178 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+12887_-12+1288 others(12): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835652 | |||||||
| chr12:51835681 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+12859T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835681 | |||||||
| chr12:51835752 | A | G | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+12788T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835752 | |||||||
| chr12:51835772 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+12768C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835772 | |||||||
| chr12:51835792 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12+12748G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835792 | |||||||
| chr12:51835805 | C | CT | 11 | a0001c0001t0003g0040 a0001c0001t0003g0073 a0001c0001t0003g0276 others(8): Show |
12 | HG02055.hp2 HG02109.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+12734dupA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835805 | |||||||
| chr12:51835805 | CT | C | 7 | a0001c0001t0002g0055 a0001c0001t0002g0109 a0001c0001t0002g0161 others(4): Show |
7 | HG01346.hp1 HG01516.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+12734delA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835805 | |||||||
| chr12:51835805 | CTT | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0020 others(107): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-12+12733_-12+1273 others(6): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51835805 | |||||||
| chr12:51836075 | C | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(258): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-12+12465G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836075 | |||||||
| chr12:51836100 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-12+12440G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836100 | |||||||
| chr12:51836269 | G | A | 1 | a0001c0001t0027g0195 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-12+12271C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836269 | |||||||
| chr12:51836339 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-12+12201C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836339 | |||||||
| chr12:51836362 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-12+12178C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836362 | |||||||
| chr12:51836410 | C | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(258): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-12+12130G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836410 | |||||||
| chr12:51836433 | A | G | 1 | a0003c0006t0008g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+12107T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836433 | |||||||
| chr12:51836584 | A | G | 10 | a0001c0001t0001g0150 a0001c0001t0003g0040 a0001c0001t0003g0276 others(7): Show |
11 | HG02055.hp2 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+11956T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836584 | |||||||
| chr12:51836585 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-12+11955C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836585 | |||||||
| chr12:51836814 | T | C | 1 | a0006c0010t0025g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+11726A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836814 | |||||||
| chr12:51836849 | G | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0100 a0001c0001t0001g0101 others(28): Show |
39 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-12+11691C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836849 | |||||||
| chr12:51836860 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+11680G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836860 | |||||||
| chr12:51836888 | G | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0276 a0001c0001t0003g0278 others(1): Show |
5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+11652C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836888 | |||||||
| chr12:51836965 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18942.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-12+11575C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51836965 | |||||||
| chr12:51837080 | A | C | 70 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(67): Show |
81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-12+11460T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837080 | |||||||
| chr12:51837115 | C | T | 1 | a0001c0001t0009g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12+11425G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837115 | |||||||
| chr12:51837300 | C | G | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+11240G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837300 | |||||||
| chr12:51837313 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-12+11227G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837313 | |||||||
| chr12:51837609 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(256): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-12+10931T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837609 | |||||||
| chr12:51837707 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+10833G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51837707 | |||||||
| chr12:51838042 | G | A | 22 | a0001c0001t0001g0285 a0001c0001t0001g0297 a0001c0001t0001g0299 others(19): Show |
24 | HG01081.hp1 HG02109.hp1 HG02735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+10498C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838042 | |||||||
| chr12:51838406 | G | A | 1 | a0001c0003t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-12+10134C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838406 | |||||||
| chr12:51838473 | G | A | 1 | a0001c0001t0003g0019 | 2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-12+10067C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838473 | |||||||
| chr12:51838571 | A | C | 1 | a0001c0003t0001g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+9969T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838571 | |||||||
| chr12:51838591 | A | T | 4 | a0002c0014t0004g0304 a0003c0006t0008g0045 a0003c0006t0008g0303 others(1): Show |
5 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+9949T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838591 | |||||||
| chr12:51838692 | A | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(203): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-12+9848T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838692 | |||||||
| chr12:51838748 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+9792G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51838748 | |||||||
| chr12:51839025 | T | G | 1 | a0001c0001t0003g0019 | 2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-12+9515A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839025 | |||||||
| chr12:51839191 | C | T | 12 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0003g0040 others(9): Show |
13 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+9349G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839191 | |||||||
| chr12:51839368 | T | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(142): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-12+9172A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839368 | |||||||
| chr12:51839432 | T | G | 3 | a0001c0003t0001g0302 a0001c0004t0005g0122 a0001c0004t0005g0291 |
3 | HG02257.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-12+9108A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839432 | |||||||
| chr12:51839475 | T | C | 3 | a0001c0003t0001g0302 a0001c0004t0005g0122 a0001c0004t0005g0291 |
3 | HG02257.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-12+9065A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839475 | |||||||
| chr12:51839662 | C | T | 1 | a0001c0004t0005g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+8878G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839662 | |||||||
| chr12:51839904 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+8636G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839904 | |||||||
| chr12:51839968 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-12+8572A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839968 | |||||||
| chr12:51839988 | CA | C | 7 | a0001c0001t0001g0297 a0001c0001t0001g0299 a0001c0001t0003g0292 others(4): Show |
8 | HG01081.hp1 HG03239.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+8551delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51839988 | |||||||
| chr12:51840378 | A | G | 181 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(178): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-12+8162T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51840378 | |||||||
| chr12:51840469 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0271 |
2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-12+8071A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51840469 | |||||||
| chr12:51840942 | T | C | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+7598A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51840942 | |||||||
| chr12:51841111 | G | C | 1 | a0001c0001t0002g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-12+7429C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841111 | |||||||
| chr12:51841197 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(300): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.-12+7343A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841197 | |||||||
| chr12:51841199 | C | T | 1 | a0001c0003t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12+7341G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841199 | |||||||
| chr12:51841238 | TG | T | 151 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0027 others(148): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-12+7301delC | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841238 | |||||||
| chr12:51841322 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-12+7218T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841322 | |||||||
| chr12:51841460 | T | G | 1 | a0002c0002t0004g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-12+7080A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841460 | |||||||
| chr12:51841477 | C | T | 1 | a0001c0003t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-12+7063G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841477 | |||||||
| chr12:51841495 | G | A | 87 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(84): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+7045C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841495 | |||||||
| chr12:51841604 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-12+6936T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841604 | |||||||
| chr12:51841606 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-12+6934T>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841606 | |||||||
| chr12:51841676 | A | G | 97 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(94): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-12+6864T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841676 | |||||||
| chr12:51841689 | G | A | 6 | a0001c0001t0001g0300 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02257.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+6851C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841689 | |||||||
| chr12:51841933 | C | G | 38 | a0001c0001t0001g0150 a0001c0001t0001g0183 a0001c0001t0001g0274 others(35): Show |
43 | HG01109.hp1 HG01243.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.-12+6607G>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841933 | |||||||
| chr12:51841993 | G | A | 15 | a0001c0001t0001g0183 a0001c0001t0002g0105 a0001c0001t0002g0107 others(12): Show |
17 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+6547C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51841993 | |||||||
| chr12:51842097 | CA | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0057 a0001c0001t0002g0118 |
4 | HG00280.hp1 HG00738.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+6442delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842097 | |||||||
| chr12:51842129 | C | T | 1 | a0002c0002t0014g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+6411G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842129 | |||||||
| chr12:51842300 | C | T | 1 | a0002c0002t0004g0233 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12+6240G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842300 | |||||||
| chr12:51842310 | G | A | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0003g0040 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+6230C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842310 | |||||||
| chr12:51842381 | T | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(102): Show |
138 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-12+6159A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842381 | |||||||
| chr12:51842674 | AATCTGCT others(27): Show |
A | 1 | a0002c0002t0004g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12+5832_-12+5865d others(36): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842674 | |||||||
| chr12:51842762 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-12+5778C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842762 | |||||||
| chr12:51842765 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-12+5775T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842765 | |||||||
| chr12:51842852 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0188 |
2 | HG00423.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-12+5688T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51842852 | |||||||
| chr12:51843044 | C | T | 1 | a0001c0003t0001g0290 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+5496G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843044 | |||||||
| chr12:51843050 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(100): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12+5490T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843050 | |||||||
| chr12:51843122 | C | T | 1 | a0001c0004t0005g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+5418G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843122 | |||||||
| chr12:51843191 | ACCCAGAG | A | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0003g0040 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+5342_-12+5348d others(9): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843191 | |||||||
| chr12:51843266 | A | C | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+5274T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843266 | |||||||
| chr12:51843275 | G | A | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+5265C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843275 | |||||||
| chr12:51843288 | A | G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(143): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-12+5252T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843288 | |||||||
| chr12:51843382 | C | CA | 92 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(89): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+5157dupT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843382 | |||||||
| chr12:51843382 | CA | C | 50 | a0001c0001t0001g0147 a0001c0001t0001g0183 a0001c0001t0001g0188 others(47): Show |
57 | HG01109.hp1 HG01243.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+5157delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843382 | |||||||
| chr12:51843382 | CAA | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(95): Show |
129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-12+5156_-12+5157d others(4): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843382 | |||||||
| chr12:51843477 | G | T | 1 | a0002c0002t0004g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+5063C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843477 | |||||||
| chr12:51843498 | A | C | 1 | a0001c0001t0003g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+5042T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843498 | |||||||
| chr12:51843544 | C | CA | 101 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(98): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-12+4995dupT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843544 | |||||||
| chr12:51843544 | CA | C | 7 | a0001c0001t0001g0147 a0001c0001t0002g0053 a0001c0001t0002g0055 others(4): Show |
7 | HG01517.hp2 HG02897.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+4995delT | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843544 | |||||||
| chr12:51843757 | T | C | 1 | a0001c0003t0001g0286 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12+4783A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843757 | |||||||
| chr12:51843811 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0188 |
2 | HG00423.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-12+4729G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843811 | |||||||
| chr12:51843921 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0002g0268 |
2 | HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-12+4619A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51843921 | |||||||
| chr12:51844000 | T | C | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0003g0040 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+4540A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844000 | |||||||
| chr12:51844061 | G | A | 1 | a0001c0004t0005g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+4479C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844061 | |||||||
| chr12:51844337 | C | T | 2 | a0001c0001t0003g0180 a0004c0005t0007g0189 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-12+4203G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844337 | |||||||
| chr12:51844513 | A | G | 1 | a0001c0003t0001g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12+4027T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844513 | |||||||
| chr12:51844554 | C | T | 19 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(16): Show |
28 | HG00597.hp1 HG02015.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+3986G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844554 | |||||||
| chr12:51844651 | G | A | 1 | a0001c0004t0005g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+3889C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844651 | |||||||
| chr12:51844712 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+3828C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844712 | |||||||
| chr12:51844743 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(194): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-12+3797T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844743 | |||||||
| chr12:51844812 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-12+3728C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51844812 | |||||||
| chr12:51845459 | C | T | 91 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(88): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+3081G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845459 | |||||||
| chr12:51845460 | G | GC | 47 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(44): Show |
55 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-12+3079dupG | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845460 | |||||||
| chr12:51845460 | G | GCC | 22 | a0001c0001t0001g0031 a0001c0001t0001g0141 a0001c0001t0001g0142 others(19): Show |
23 | HG00408.hp1 HG00544.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+3078_-12+3079d others(4): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845460 | |||||||
| chr12:51845460 | GC | G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(127): Show |
167 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-12+3079delG | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845460 | |||||||
| chr12:51845468 | C | A | 1 | a0002c0002t0016g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+3072G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845468 | |||||||
| chr12:51845480 | G | GGTGGGGG others(29): Show |
1 | a0002c0002t0004g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12+3059_-12+3060i others(38): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845480 | |||||||
| chr12:51845481 | T | G | 1 | a0002c0002t0004g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12+3059A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845481 | |||||||
| chr12:51845545 | C | T | 9 | a0001c0001t0001g0285 a0001c0003t0001g0116 a0001c0003t0001g0281 others(6): Show |
10 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+2995G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845545 | |||||||
| chr12:51845607 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12+2933G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845607 | |||||||
| chr12:51845627 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(54): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+2913G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845627 | |||||||
| chr12:51845773 | CT | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(197): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-12+2766delA | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845773 | |||||||
| chr12:51845792 | G | A | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+2748C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845792 | |||||||
| chr12:51845969 | C | T | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+2571G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845969 | |||||||
| chr12:51845970 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(290): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-12+2570T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845970 | |||||||
| chr12:51845992 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-12+2548C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51845992 | |||||||
| chr12:51846021 | A | G | 1 | a0001c0004t0005g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-12+2519T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846021 | |||||||
| chr12:51846150 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+2390G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846150 | |||||||
| chr12:51846394 | G | A | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+2146C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846394 | |||||||
| chr12:51846504 | T | C | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0003g0040 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+2036A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846504 | |||||||
| chr12:51846722 | G | A | 5 | a0001c0001t0003g0138 a0001c0003t0006g0005 a0001c0003t0006g0137 others(2): Show |
8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+1818C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846722 | |||||||
| chr12:51846861 | A | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0141 a0001c0001t0001g0142 |
4 | HG02074.hp2 NA18951.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1679T>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846861 | |||||||
| chr12:51846926 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-12+1614T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51846926 | |||||||
| chr12:51847001 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-12+1539G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847001 | |||||||
| chr12:51847044 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-12+1496C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847044 | |||||||
| chr12:51847128 | G | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0276 a0001c0001t0003g0278 others(1): Show |
5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1412C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847128 | |||||||
| chr12:51847196 | A | G | 2 | a0001c0003t0001g0042 a0001c0003t0001g0279 |
3 | HG03491.hp1 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-12+1344T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847196 | |||||||
| chr12:51847380 | G | A | 1 | a0004c0005t0007g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-12+1160C>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847380 | |||||||
| chr12:51847391 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+1149A>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847391 | |||||||
| chr12:51847546 | C | T | 1 | a0002c0002t0004g0018 | 2 | NA18950.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-12+994G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847546 | |||||||
| chr12:51847560 | CCCACCCA others(5): Show |
C | 1 | a0001c0001t0001g0041 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.-12+968_-12+979del others(12): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847560 | |||||||
| chr12:51847725 | A | G | 9 | a0001c0001t0001g0204 a0001c0001t0002g0033 a0001c0001t0002g0203 others(6): Show |
10 | HG01928.hp1 HG01934.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+815T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847725 | |||||||
| chr12:51847771 | G | C | 4 | a0001c0001t0010g0015 a0001c0001t0010g0049 a0001c0020t0017g0048 others(1): Show |
5 | HG02622.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+769C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847771 | |||||||
| chr12:51847792 | T | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0190 a0001c0001t0001g0191 others(6): Show |
10 | HG01952.hp2 HG01981.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+748A>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847792 | |||||||
| chr12:51847922 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0069 others(99): Show |
133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-12+618G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847922 | |||||||
| chr12:51847930 | T | C | 24 | a0001c0001t0001g0300 a0001c0001t0001g0316 a0001c0001t0001g0317 others(21): Show |
26 | HG01109.hp1 HG01243.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.-12+610A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51847930 | |||||||
| chr12:51848083 | C | CCA | 102 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(99): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-12+455_-12+456dup others(2): Show |
FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848083 | |||||||
| chr12:51848149 | C | T | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+391G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848149 | |||||||
| chr12:51848181 | C | T | 1 | a0002c0002t0004g0017 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-12+359G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848181 | |||||||
| chr12:51848283 | G | T | 2 | a0002c0002t0004g0025 a0002c0002t0004g0119 |
3 | HG00639.hp1 HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-12+257C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848283 | |||||||
| chr12:51848316 | G | C | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+224C>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848316 | |||||||
| chr12:51848321 | G | T | 2 | a0001c0001t0003g0325 a0001c0004t0005g0324 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+219C>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848321 | |||||||
| chr12:51848322 | C | T | 2 | a0001c0001t0003g0325 a0001c0004t0005g0324 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+218G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848322 | |||||||
| chr12:51848339 | A | G | 277 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(274): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-12+201T>C | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848339 | |||||||
| chr12:51848409 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0051 |
3 | HG01934.hp2 HG02280.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-12+131G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848409 | |||||||
| chr12:51848423 | T | C | 2 | a0001c0001t0013g0322 a0004c0005t0007g0323 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+117A>G | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848423 | |||||||
| chr12:51848477 | C | T | 79 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0074 others(76): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+63G>A | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848477 | |||||||
| chr12:51848490 | C | A | 2 | a0001c0001t0003g0325 a0001c0004t0005g0324 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+50G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848490 | |||||||
| chr12:51848507 | C | A | 2 | a0001c0001t0002g0047 a0002c0002t0004g0326 |
3 | HG03654.hp1 NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-12+33G>T | FIGNL2 | ENSG00000261308.4 | transcript | ENST00000618634.3 | protein_coding | 1/1 | chr12 | 51848507 |