Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2346 |
| ensemblid | ENSG00000086205.18 |
| hgncid | 3788 |
| symbol | FOLH1 |
| name | folate hydrolase 1 |
| refseq_nuc | NM_004476.3 |
| refseq_prot | NP_004467.1 |
| ensembl_nuc | ENST00000256999.7 |
| ensembl_prot | ENSP00000256999.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 49145092 |
| end | 49208602 |
| strand | - |
| ver | v1.2 |
| region | chr11:49145092-49208602 |
| region5000 | chr11:49140092-49213602 |
| regionname0 | FOLH1_chr11_49145092_49208602 |
| regionname5000 | FOLH1_chr11_49140092_49213602 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 750 | 195 | 35 | 39 | 92 | 11 | 17 | 70 | FOLH1_chr11_49140092_49213602 | FOLH1 | MWNLL others(745): Show |
chr11 | 49140092 | 49213602 |
| a0002 | 0/1 | 750 | 166 | 50 | 21 | 74 | 5 | 15 | 56 | FOLH1_chr11_49140092_49213602 | FOLH1 | MWNLL others(745): Show |
chr11 | 49140092 | 49213602 |
| a0003 | 0/0 | 749 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | MWNLH others(744): Show |
chr11 | 49140092 | 49213602 |
| a0004 | 0/0 | 750 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | MWNLL others(745): Show |
chr11 | 49140092 | 49213602 |
| a0005 | 0/0 | 750 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | MWNLL others(745): Show |
chr11 | 49140092 | 49213602 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2250 | 184 | 27 | 37 | 92 | 11 | 16 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0001c0004 | 0/0 | 2250 | 8 | 8 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0001c0008 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0001c0009 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0001c0010 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0002c0002 | 0/1 | 2250 | 99 | 50 | 11 | 33 | 0 | 4 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0002c0003 | 0/0 | 2250 | 66 | 0 | 9 | 41 | 5 | 11 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0002c0011 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0003c0005 | 0/0 | 2247 | 6 | 5 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2242): Show |
chr11 | 49140092 | 49213602 | ||
| a0004c0006 | 0/0 | 2250 | 5 | 5 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 | ||
| a0005c0007 | 0/0 | 2250 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | ATGTG others(2245): Show |
chr11 | 49140092 | 49213602 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4110 | 40 | 11 | 8 | 14 | 4 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0002 | 0/0 | 4110 | 131 | 13 | 26 | 75 | 4 | 13 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0005 | 0/0 | 4110 | 5 | 0 | 3 | 0 | 2 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0007 | 0/0 | 4110 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0011 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0012 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0014 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0015 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0001t0016 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0004t0001 | 0/0 | 4110 | 8 | 8 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0008t0002 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0009t0002 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0001c0010t0002 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0001 | 0/0 | 4110 | 26 | 26 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0002 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0003 | 0/1 | 4110 | 66 | 19 | 11 | 33 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0004 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0008 | 0/0 | 4110 | 3 | 1 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0002t0010 | 0/0 | 4110 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0003t0001 | 0/0 | 4110 | 64 | 0 | 9 | 40 | 4 | 11 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0003t0002 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0003t0013 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0002c0011t0001 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0003c0005t0002 | 0/0 | 4107 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4102): Show |
chr11 | 49140092 | 49213602 |
| a0003c0005t0006 | 0/0 | 4107 | 4 | 4 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4102): Show |
chr11 | 49140092 | 49213602 |
| a0004c0006t0004 | 0/0 | 4110 | 5 | 5 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| a0005c0007t0009 | 0/0 | 4110 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | AGTGC others(4105): Show |
chr11 | 49140092 | 49213602 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0001t0016g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0008t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0009t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0001c0010t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0002t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0003t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0002c0011t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0003c0005t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0003c0005t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0003c0005t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0003c0005t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0003c0005t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0004c0006t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0004c0006t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0004c0006t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0004c0006t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0005c0007t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| a0005c0007t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0212 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0062 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0170 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | FIN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0281 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00597 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0272 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0057 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0283 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0084 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0033 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0054 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01109 | hp1 | a0003 | c0005 | t0002 | g0030 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01109 | hp2 | a0002 | c0011 | t0001 | g0312 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01168 | hp1 | a0001 | c0008 | t0002 | g0213 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01175 | hp2 | a0001 | c0010 | t0002 | g0210 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0252 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0304 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01346 | hp2 | a0005 | c0007 | t0009 | g0243 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0070 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0073 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0266 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01515 | hp2 | a0001 | c0001 | t0015 | g0324 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0064 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0061 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01884 | hp1 | a0003 | c0005 | t0006 | g0028 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0071 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0284 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0086 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0068 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02040 | hp2 | a0002 | c0002 | t0003 | g0271 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02055 | hp1 | a0003 | c0005 | t0006 | g0327 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0259 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02074 | hp1 | a0002 | c0002 | t0003 | g0285 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02135 | hp2 | a0001 | c0001 | t0014 | g0180 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0315 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0254 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0069 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0299 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0032 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02602 | hp2 | a0001 | c0009 | t0002 | g0169 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02615 | hp1 | a0004 | c0006 | t0004 | g0318 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02615 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02622 | hp1 | a0004 | c0006 | t0004 | g0026 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0102 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0248 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02698 | hp1 | a0002 | c0002 | t0008 | g0258 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02717 | hp2 | a0004 | c0006 | t0004 | g0026 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0072 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0112 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0261 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0267 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0251 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0108 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0298 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0257 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0256 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0307 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02976 | hp1 | a0003 | c0005 | t0002 | g0029 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0297 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0301 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0063 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03453 | hp2 | a0004 | c0006 | t0004 | g0320 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0311 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0255 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0262 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03492 | hp2 | a0002 | c0002 | t0008 | g0275 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0253 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0310 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03579 | hp1 | a0002 | c0002 | t0004 | g0313 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0059 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0277 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0058 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03942 | hp2 | a0001 | c0001 | t0012 | g0184 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0074 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0075 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18522 | hp1 | a0002 | c0002 | t0010 | g0249 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18939 | hp1 | a0002 | c0003 | t0013 | g0046 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0286 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0282 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0270 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0278 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18947 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0274 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0269 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18959 | hp1 | a0002 | c0002 | t0003 | g0276 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18975 | hp1 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0280 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18987 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18991 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18993 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0268 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19062 | hp1 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19062 | hp2 | a0002 | c0002 | t0003 | g0279 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19076 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19078 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19082 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0273 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19088 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19090 | hp1 | a0001 | c0001 | t0016 | g0325 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA19240 | hp2 | a0003 | c0005 | t0006 | g0326 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ASW | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20129 | hp2 | a0005 | c0007 | t0009 | g0244 | AFR | ASW | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0055 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0049 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | GIH | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02109 | hp2 | a0002 | c0002 | t0008 | g0265 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0247 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG02559 | hp2 | a0003 | c0005 | t0006 | g0028 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0010 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG03471 | hp2 | a0004 | c0006 | t0004 | g0319 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20300 | hp1 | a0002 | c0002 | t0010 | g0250 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0264 | REF | REF | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0181 | REF | REF | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:49164722 | G | A | 2 | a0004 a0005 |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.1423C>T | p.His475Tyr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/19 | 1616/4110 | 1423/2253 | 475/750 | chr11 | 49164722 | |||
| chr11:49192842 | G | A | 1 | a0004 | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.464C>T | p.Ser155Leu | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/19 | 657/4110 | 464/2253 | 155/750 | chr11 | 49192842 | |||
| chr11:49206068 | A | G | 1 | a0002 | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
missense_variant&splice_region_variant | MODERATE | c.223T>C | p.Tyr75His | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/19 | 416/4110 | 223/2253 | 75/750 | chr11 | 49206068 | |||
| chr11:49208393 | TGAA | T | 1 | a0003 | 6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.14_16delTTC | p.Leu5del | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 209/4110 | 14/2253 | 5/750 | chr11 | 49208393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:49146864 | A | G | 1 | a0001c0009 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2145T>C | p.Ile715Ile | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 2338/4110 | 2145/2253 | 715/750 | chr11 | 49146864 | |||
| chr11:49153923 | T | C | 1 | a0001c0010 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1893A>G | p.Ser631Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/19 | 2086/4110 | 1893/2253 | 631/750 | chr11 | 49153923 | |||
| chr11:49174938 | T | C | 5 | a0001c0004 a0002c0002 a0002c0003 others(2): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
synonymous_variant | LOW | c.1059A>G | p.Thr353Thr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/19 | 1252/4110 | 1059/2253 | 353/750 | chr11 | 49174938 | |||
| chr11:49175864 | A | G | 2 | a0001c0004 a0002c0003 |
74 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.1014T>C | p.Ser338Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/19 | 1207/4110 | 1014/2253 | 338/750 | chr11 | 49175864 | |||
| chr11:49185763 | A | G | 4 | a0002c0002 a0002c0003 a0002c0011 others(1): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
synonymous_variant | LOW | c.732T>C | p.Asp244Asp | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/19 | 925/4110 | 732/2253 | 244/750 | chr11 | 49185763 | |||
| chr11:49186746 | A | G | 1 | a0001c0008 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.537T>C | p.Tyr179Tyr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/19 | 730/4110 | 537/2253 | 179/750 | chr11 | 49186746 | |||
| chr11:49200333 | T | A | 5 | a0002c0002 a0002c0003 a0002c0011 others(2): Show |
172 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(169): Show |
synonymous_variant | LOW | c.333A>T | p.Ala111Ala | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/19 | 526/4110 | 333/2253 | 111/750 | chr11 | 49200333 | |||
| chr11:49200339 | C | T | 1 | a0002c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.327G>A | p.Glu109Glu | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/19 | 520/4110 | 327/2253 | 109/750 | chr11 | 49200339 | |||
| chr11:49206156 | G | A | 1 | a0002c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/19 | 328/4110 | 135/2253 | 45/750 | chr11 | 49206156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:49145177 | C | T | 1 | a0002c0003t0013 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1579 | chr11 | 49145177 | ||||||
| chr11:49145178 | A | G | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(11): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1578T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1578 | chr11 | 49145178 | ||||||
| chr11:49145304 | C | G | 1 | a0005c0007t0009 | 2 | HG01346.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1452 | chr11 | 49145304 | ||||||
| chr11:49145386 | T | C | 1 | a0002c0002t0010 | 2 | NA18522.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1370A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1370 | chr11 | 49145386 | ||||||
| chr11:49145600 | G | A | 1 | a0001c0001t0014 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1156C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1156 | chr11 | 49145600 | ||||||
| chr11:49145863 | G | A | 2 | a0002c0002t0004 a0004c0006t0004 |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 893 | chr11 | 49145863 | ||||||
| chr11:49146084 | T | C | 2 | a0002c0002t0004 a0004c0006t0004 |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*672A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 672 | chr11 | 49146084 | ||||||
| chr11:49146109 | T | C | 1 | a0001c0001t0015 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 647 | chr11 | 49146109 | ||||||
| chr11:49146356 | C | T | 1 | a0001c0001t0012 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 400 | chr11 | 49146356 | ||||||
| chr11:49146400 | G | A | 1 | a0001c0001t0005 | 5 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*356C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 356 | chr11 | 49146400 | ||||||
| chr11:49146414 | A | G | 1 | a0001c0001t0011 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 342 | chr11 | 49146414 | ||||||
| chr11:49146464 | C | G | 1 | a0002c0002t0008 | 3 | HG02109.hp2 HG02698.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 292 | chr11 | 49146464 | ||||||
| chr11:49146626 | T | C | 1 | a0001c0001t0007 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*130A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 130 | chr11 | 49146626 | ||||||
| chr11:49146748 | G | A | 3 | a0002c0002t0003 a0002c0002t0008 a0002c0002t0010 |
70 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 8 | chr11 | 49146748 | ||||||
| chr11:49208425 | G | A | 1 | a0001c0001t0016 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 16 | chr11 | 49208425 | ||||||
| chr11:49208591 | C | A | 1 | a0003c0005t0006 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-182G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 182 | chr11 | 49208591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:49146960 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064-15C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49146960 | |||||||
| chr11:49147060 | T | C | 52 | a0002c0002t0003g0001 a0002c0002t0003g0010 a0002c0002t0003g0011 others(49): Show |
70 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2064-115A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147060 | |||||||
| chr11:49147159 | G | C | 6 | a0002c0002t0001g0307 a0002c0002t0001g0308 a0002c0002t0001g0309 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064-214C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147159 | |||||||
| chr11:49147241 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2064-296T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147241 | |||||||
| chr11:49147267 | T | C | 5 | a0002c0003t0001g0051 a0002c0003t0001g0068 a0002c0003t0001g0069 others(2): Show |
5 | HG01361.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064-322A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147267 | |||||||
| chr11:49147446 | GT | G | 287 | a0001c0001t0001g0229 a0001c0001t0002g0002 a0001c0001t0002g0005 others(284): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.2064-502delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147446 | |||||||
| chr11:49147734 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0316 |
3 | HG02896.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2064-789G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147734 | |||||||
| chr11:49147755 | C | A | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2064-810G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147755 | |||||||
| chr11:49147931 | GA | G | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2063+707delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147931 | |||||||
| chr11:49148234 | A | G | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2063+405T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49148234 | |||||||
| chr11:49148301 | T | C | 68 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(65): Show |
73 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2063+338A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49148301 | |||||||
| chr11:49148782 | T | C | 289 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(286): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1971-51A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49148782 | |||||||
| chr11:49148979 | G | A | 1 | a0002c0002t0003g0276 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1971-248C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49148979 | |||||||
| chr11:49149038 | A | G | 1 | a0002c0002t0001g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1971-307T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149038 | |||||||
| chr11:49149114 | G | C | 1 | a0001c0001t0002g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1971-383C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149114 | |||||||
| chr11:49149116 | T | G | 45 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0098 others(42): Show |
49 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1971-385A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149116 | |||||||
| chr11:49149222 | T | C | 91 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(88): Show |
96 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1971-491A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149222 | |||||||
| chr11:49149423 | G | T | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1971-692C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149423 | |||||||
| chr11:49149538 | G | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1971-807C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149538 | |||||||
| chr11:49149744 | T | A | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1971-1013A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149744 | |||||||
| chr11:49149870 | G | A | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971-1139C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149870 | |||||||
| chr11:49149997 | G | A | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1971-1266C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149997 | |||||||
| chr11:49150113 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1971-1382A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150113 | |||||||
| chr11:49150138 | T | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1971-1407A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150138 | |||||||
| chr11:49150162 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1971-1431G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150162 | |||||||
| chr11:49150169 | T | C | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(126): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1971-1438A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150169 | |||||||
| chr11:49150203 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1971-1472A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150203 | |||||||
| chr11:49150290 | C | T | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1971-1559G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150290 | |||||||
| chr11:49150397 | T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1971-1666A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150397 | |||||||
| chr11:49150442 | A | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1971-1711T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150442 | |||||||
| chr11:49150463 | C | G | 1 | a0002c0003t0001g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1971-1732G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150463 | |||||||
| chr11:49150519 | T | C | 4 | a0001c0001t0007g0008 a0003c0005t0006g0028 a0003c0005t0006g0326 others(1): Show |
7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1971-1788A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150519 | |||||||
| chr11:49150571 | T | C | 1 | a0002c0002t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1971-1840A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150571 | |||||||
| chr11:49150867 | G | A | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1971-2136C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150867 | |||||||
| chr11:49151137 | G | A | 8 | a0002c0002t0001g0307 a0002c0002t0001g0308 a0002c0002t0001g0309 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1971-2406C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151137 | |||||||
| chr11:49151375 | C | CAT | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1970+2470_1970+247 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151375 | |||||||
| chr11:49151389 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970+2457G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151389 | |||||||
| chr11:49151390 | G | A | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1970+2456C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151390 | |||||||
| chr11:49151397 | C | T | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1970+2449G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151397 | |||||||
| chr11:49151407 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1970+2439G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151407 | |||||||
| chr11:49151408 | G | A | 38 | a0002c0003t0001g0013 a0002c0003t0001g0031 a0002c0003t0001g0035 others(35): Show |
39 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1970+2438C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151408 | |||||||
| chr11:49151414 | G | GCA | 3 | a0002c0003t0001g0084 a0002c0003t0001g0085 a0002c0003t0001g0086 |
3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1970+2430_1970+243 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151414 | |||||||
| chr11:49151427 | C | CACAG | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+2418_1970+241 others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151427 | |||||||
| chr11:49151429 | G | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+2417C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151429 | |||||||
| chr11:49151429 | GAC | G | 55 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(52): Show |
73 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1970+2415_1970+241 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151429 | |||||||
| chr11:49151601 | C | CTAT | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1970+2242_1970+224 others(7): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151601 | |||||||
| chr11:49151682 | T | C | 135 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(132): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1970+2164A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151682 | |||||||
| chr11:49151779 | A | G | 286 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(283): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1970+2067T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151779 | |||||||
| chr11:49151804 | T | G | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1970+2042A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151804 | |||||||
| chr11:49151885 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+1961A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151885 | |||||||
| chr11:49151956 | C | T | 1 | a0002c0003t0001g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1970+1890G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151956 | |||||||
| chr11:49152047 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1970+1799G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152047 | |||||||
| chr11:49152048 | A | G | 4 | a0002c0002t0003g0021 a0002c0002t0003g0247 a0002c0002t0003g0248 others(1): Show |
5 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1970+1798T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152048 | |||||||
| chr11:49152074 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1970+1772T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152074 | |||||||
| chr11:49152327 | T | G | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+1519A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152327 | |||||||
| chr11:49152455 | A | C | 130 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(127): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1970+1391T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152455 | |||||||
| chr11:49152589 | G | T | 289 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(286): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1970+1257C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152589 | |||||||
| chr11:49152616 | G | A | 1 | a0002c0002t0003g0298 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1970+1230C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152616 | |||||||
| chr11:49152692 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1970+1154G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152692 | |||||||
| chr11:49152751 | C | T | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1970+1095G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152751 | |||||||
| chr11:49152792 | T | C | 3 | a0002c0002t0003g0263 a0002c0002t0003g0274 a0002c0002t0003g0278 |
3 | NA18946.hp1 NA18953.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1970+1054A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152792 | |||||||
| chr11:49152815 | T | C | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1970+1031A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152815 | |||||||
| chr11:49152886 | T | C | 6 | a0001c0001t0007g0008 a0003c0005t0002g0029 a0003c0005t0002g0030 others(3): Show |
9 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1970+960A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152886 | |||||||
| chr11:49153106 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1970+740A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153106 | |||||||
| chr11:49153390 | T | C | 286 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(283): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1970+456A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153390 | |||||||
| chr11:49153600 | G | C | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1970+246C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153600 | |||||||
| chr11:49153691 | T | C | 1 | a0002c0002t0003g0270 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1970+155A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153691 | |||||||
| chr11:49153704 | C | G | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+142G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153704 | |||||||
| chr11:49153999 | A | G | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1889-72T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 16/18 | chr11 | 49153999 | |||||||
| chr11:49154505 | C | T | 141 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(138): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1624-13G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154505 | |||||||
| chr11:49154506 | A | G | 22 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0032 others(19): Show |
26 | HG00597.hp1 HG00609.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1624-14T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154506 | |||||||
| chr11:49154591 | G | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1624-99C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154591 | |||||||
| chr11:49154626 | A | G | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1624-134T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154626 | |||||||
| chr11:49154675 | A | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1624-183T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154675 | |||||||
| chr11:49154714 | T | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-222A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154714 | |||||||
| chr11:49154759 | G | A | 2 | a0002c0003t0001g0031 a0002c0003t0001g0037 |
2 | NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1624-267C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154759 | |||||||
| chr11:49154806 | A | T | 3 | a0001c0001t0002g0141 a0001c0001t0002g0195 a0001c0001t0002g0196 |
3 | HG00558.hp1 NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1624-314T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154806 | |||||||
| chr11:49154933 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1624-441T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154933 | |||||||
| chr11:49154952 | A | G | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1624-460T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154952 | |||||||
| chr11:49155393 | A | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1624-901T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155393 | |||||||
| chr11:49155501 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1624-1009T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155501 | |||||||
| chr11:49155597 | G | T | 1 | a0001c0001t0002g0134 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1624-1105C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155597 | |||||||
| chr11:49155695 | A | T | 92 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(89): Show |
97 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1623+1022T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155695 | |||||||
| chr11:49155795 | C | CAT | 44 | a0001c0001t0001g0122 a0001c0001t0001g0221 a0001c0001t0001g0225 others(41): Show |
48 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1623+920_1623+921d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATAT | 43 | a0001c0001t0001g0020 a0001c0001t0001g0219 a0001c0001t0001g0220 others(40): Show |
47 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1623+918_1623+921d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATATAT | 52 | a0001c0001t0001g0019 a0001c0001t0001g0218 a0001c0001t0001g0223 others(49): Show |
62 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1623+916_1623+921d others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATATATA others(1): Show |
45 | a0001c0001t0001g0009 a0001c0001t0001g0222 a0001c0001t0001g0242 others(42): Show |
48 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1623+914_1623+921d others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATATATA others(3): Show |
22 | a0001c0001t0001g0226 a0001c0001t0002g0089 a0001c0001t0002g0105 others(19): Show |
22 | HG01168.hp1 HG01175.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1623+912_1623+921d others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATATATA others(5): Show |
10 | a0001c0001t0002g0145 a0001c0001t0002g0179 a0001c0001t0002g0187 others(7): Show |
10 | HG00597.hp1 HG01993.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.1623+910_1623+921d others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | C | CATATATA others(7): Show |
3 | a0001c0001t0002g0144 a0002c0003t0001g0072 a0002c0003t0002g0049 |
3 | HG00280.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1623+908_1623+921d others(16): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CAT | C | 4 | a0001c0001t0002g0175 a0002c0002t0001g0308 a0002c0002t0001g0311 others(1): Show |
4 | HG00735.hp1 HG01346.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623+920_1623+921d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATAT | C | 6 | a0002c0002t0001g0300 a0002c0002t0001g0309 a0002c0002t0001g0310 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1623+918_1623+921d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(1): Show |
C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0101 a0001c0001t0002g0165 others(4): Show |
10 | HG02109.hp1 HG02293.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1623+914_1623+921d others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1623+912_1623+921d others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(5): Show |
C | 5 | a0001c0001t0002g0119 a0002c0002t0004g0313 a0004c0006t0004g0026 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+910_1623+921d others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(7): Show |
C | 3 | a0002c0002t0001g0305 a0002c0002t0001g0306 a0002c0011t0001g0312 |
3 | HG01109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1623+908_1623+921d others(16): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(9): Show |
C | 5 | a0002c0002t0003g0248 a0002c0002t0003g0252 a0002c0002t0003g0253 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+906_1623+921d others(18): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(11): Show |
C | 48 | a0001c0001t0001g0238 a0002c0002t0002g0268 a0002c0002t0003g0001 others(45): Show |
66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1623+904_1623+921d others(20): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155795 | CATATATA others(13): Show |
C | 2 | a0001c0001t0002g0183 a0002c0002t0003g0272 |
2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1623+902_1623+921d others(22): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | |||||||
| chr11:49155835 | T | TATATATA others(3): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0322 a0002c0002t0001g0307 |
4 | HG02559.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+881_1623+882i others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155835 | |||||||
| chr11:49155835 | T | TATATATA others(5): Show |
1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1623+881_1623+882i others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155835 | |||||||
| chr11:49155842 | C | T | 3 | a0001c0001t0002g0095 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02280.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1623+875G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155842 | |||||||
| chr11:49155967 | C | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1623+750G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155967 | |||||||
| chr11:49156124 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+593A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156124 | |||||||
| chr11:49156256 | T | C | 13 | a0001c0001t0007g0008 a0002c0002t0004g0313 a0003c0005t0002g0029 others(10): Show |
17 | HG01109.hp1 HG01346.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1623+461A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156256 | |||||||
| chr11:49156311 | A | G | 4 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623+406T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156311 | |||||||
| chr11:49156367 | T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1623+350A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156367 | |||||||
| chr11:49156545 | A | C | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+172T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156545 | |||||||
| chr11:49156551 | T | C | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+166A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156551 | |||||||
| chr11:49156588 | T | C | 16 | a0001c0001t0002g0017 a0001c0001t0002g0115 a0001c0001t0002g0125 others(13): Show |
17 | HG00544.hp1 HG02300.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.1623+129A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156588 | |||||||
| chr11:49156702 | T | C | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+15A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156702 | |||||||
| chr11:49156921 | A | G | 1 | a0002c0002t0003g0282 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1533-114T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49156921 | |||||||
| chr11:49156929 | A | G | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-122T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49156929 | |||||||
| chr11:49157105 | C | T | 2 | a0002c0002t0003g0256 a0002c0002t0003g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1533-298G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157105 | |||||||
| chr11:49157352 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1533-545G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157352 | |||||||
| chr11:49157465 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1532+487T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157465 | |||||||
| chr11:49157539 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1532+413A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157539 | |||||||
| chr11:49157596 | C | G | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1532+356G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157596 | |||||||
| chr11:49157737 | C | T | 92 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(89): Show |
97 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1532+215G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157737 | |||||||
| chr11:49157838 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1532+114C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157838 | |||||||
| chr11:49157858 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1532+94G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157858 | |||||||
| chr11:49158044 | C | T | 1 | a0002c0002t0010g0249 | 1 | NA18522.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1441-1G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158044 | |||||||
| chr11:49158177 | C | T | 3 | a0002c0003t0001g0084 a0002c0003t0001g0085 a0002c0003t0001g0086 |
3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1441-134G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158177 | |||||||
| chr11:49158256 | T | C | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1441-213A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158256 | |||||||
| chr11:49158288 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1441-245G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158288 | |||||||
| chr11:49158436 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1441-393C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158436 | |||||||
| chr11:49158556 | G | T | 128 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(125): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1441-513C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158556 | |||||||
| chr11:49158633 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-590A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158633 | |||||||
| chr11:49158717 | T | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1441-674A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158717 | |||||||
| chr11:49158731 | G | A | 1 | a0002c0003t0001g0037 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1441-688C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158731 | |||||||
| chr11:49158908 | G | T | 7 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(4): Show |
8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-865C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158908 | |||||||
| chr11:49158975 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-932A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158975 | |||||||
| chr11:49159056 | T | C | 134 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(131): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1441-1013A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159056 | |||||||
| chr11:49159284 | A | G | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1441-1241T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159284 | |||||||
| chr11:49159356 | T | C | 5 | a0002c0002t0004g0313 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-1313A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159356 | |||||||
| chr11:49159875 | G | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-1832C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159875 | |||||||
| chr11:49159906 | C | CT | 7 | a0001c0001t0002g0130 a0002c0002t0003g0274 a0002c0002t0003g0297 others(4): Show |
8 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-1864dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159906 | |||||||
| chr11:49159906 | CT | C | 29 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0016 others(26): Show |
34 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1441-1864delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159906 | |||||||
| chr11:49159960 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(4): Show |
8 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-1917A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159960 | |||||||
| chr11:49160014 | G | A | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1441-1971C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160014 | |||||||
| chr11:49160037 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-1994G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160037 | |||||||
| chr11:49160040 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1441-1997C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160040 | |||||||
| chr11:49160374 | G | T | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1441-2331C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160374 | |||||||
| chr11:49160444 | T | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2401A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160444 | |||||||
| chr11:49160503 | C | T | 1 | a0002c0002t0003g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1441-2460G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160503 | |||||||
| chr11:49160504 | G | A | 4 | a0002c0002t0003g0011 a0002c0002t0003g0276 a0002c0002t0003g0283 others(1): Show |
6 | HG00733.hp1 HG01081.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-2461C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160504 | |||||||
| chr11:49160593 | C | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2550G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160593 | |||||||
| chr11:49160635 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1441-2592C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160635 | |||||||
| chr11:49160741 | C | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1441-2698G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160741 | |||||||
| chr11:49160742 | A | G | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1441-2699T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160742 | |||||||
| chr11:49160873 | T | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2830A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160873 | |||||||
| chr11:49160911 | G | A | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1441-2868C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160911 | |||||||
| chr11:49160923 | A | C | 2 | a0002c0002t0003g0256 a0002c0002t0003g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1441-2880T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160923 | |||||||
| chr11:49160982 | G | A | 1 | a0002c0003t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1441-2939C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160982 | |||||||
| chr11:49160995 | A | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1441-2952T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160995 | |||||||
| chr11:49160996 | C | T | 1 | a0002c0002t0003g0024 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1441-2953G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160996 | |||||||
| chr11:49161008 | C | A | 1 | a0001c0001t0012g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1441-2965G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161008 | |||||||
| chr11:49161096 | C | T | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1441-3053G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161096 | |||||||
| chr11:49161392 | T | C | 2 | a0003c0005t0002g0029 a0003c0005t0002g0030 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1440+3313A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161392 | |||||||
| chr11:49161397 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1440+3308A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161397 | |||||||
| chr11:49161402 | T | A | 1 | a0001c0001t0002g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1440+3303A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161402 | |||||||
| chr11:49161515 | T | C | 1 | a0002c0003t0001g0038 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1440+3190A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161515 | |||||||
| chr11:49161664 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1440+3041A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161664 | |||||||
| chr11:49161741 | GT | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+2963delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161741 | |||||||
| chr11:49161852 | T | G | 1 | a0002c0002t0004g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1440+2853A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161852 | |||||||
| chr11:49161854 | A | G | 128 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(125): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1440+2851T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161854 | |||||||
| chr11:49161951 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1440+2754G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161951 | |||||||
| chr11:49162014 | C | T | 1 | a0001c0001t0011g0142 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1440+2691G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162014 | |||||||
| chr11:49162189 | AG | A | 4 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+2515delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162189 | |||||||
| chr11:49162535 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1440+2170G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162535 | |||||||
| chr11:49162617 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1440+2088C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162617 | |||||||
| chr11:49162619 | T | C | 5 | a0002c0002t0002g0268 a0002c0002t0003g0022 a0002c0002t0003g0261 others(2): Show |
6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+2086A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162619 | |||||||
| chr11:49162753 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1440+1952C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162753 | |||||||
| chr11:49162810 | G | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+1895C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162810 | |||||||
| chr11:49162837 | G | A | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1440+1868C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162837 | |||||||
| chr11:49162854 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1440+1851G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162854 | |||||||
| chr11:49162959 | C | T | 1 | a0002c0002t0003g0304 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1440+1746G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162959 | |||||||
| chr11:49163036 | T | C | 1 | a0002c0002t0003g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1440+1669A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163036 | |||||||
| chr11:49163649 | A | G | 139 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(136): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1440+1056T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163649 | |||||||
| chr11:49163697 | G | A | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1440+1008C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163697 | |||||||
| chr11:49163760 | T | C | 6 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(3): Show |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+945A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163760 | |||||||
| chr11:49163855 | C | T | 7 | a0001c0001t0002g0014 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
8 | HG00438.hp1 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440+850G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163855 | |||||||
| chr11:49163862 | G | A | 54 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(51): Show |
58 | HG00597.hp1 HG00609.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1440+843C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163862 | |||||||
| chr11:49163887 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0162 |
2 | HG01358.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1440+818A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163887 | |||||||
| chr11:49163929 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1440+776C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163929 | |||||||
| chr11:49163972 | C | T | 128 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(125): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1440+733G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163972 | |||||||
| chr11:49164022 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1440+683A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164022 | |||||||
| chr11:49164054 | T | C | 4 | a0002c0002t0003g0001 a0002c0002t0003g0273 a0002c0002t0003g0277 others(1): Show |
12 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440+651A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164054 | |||||||
| chr11:49164370 | G | A | 5 | a0001c0001t0002g0017 a0001c0001t0002g0156 a0001c0001t0002g0172 others(2): Show |
6 | NA18939.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+335C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164370 | |||||||
| chr11:49164405 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1440+300T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164405 | |||||||
| chr11:49164449 | C | T | 1 | a0002c0002t0010g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1440+256G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164449 | |||||||
| chr11:49164639 | C | CATA | 6 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(3): Show |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+63_1440+65dup others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164639 | |||||||
| chr11:49164911 | C | G | 1 | a0002c0002t0001g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1373-139G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49164911 | |||||||
| chr11:49164918 | T | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0164 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1373-146A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49164918 | |||||||
| chr11:49165038 | G | T | 6 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(3): Show |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-266C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165038 | |||||||
| chr11:49165101 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-329G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165101 | |||||||
| chr11:49165129 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-357G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165129 | |||||||
| chr11:49165163 | C | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1373-391G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165163 | |||||||
| chr11:49165204 | G | T | 1 | a0001c0001t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1373-432C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165204 | |||||||
| chr11:49165225 | A | C | 1 | a0002c0011t0001g0312 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1373-453T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165225 | |||||||
| chr11:49165346 | T | G | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-574A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165346 | |||||||
| chr11:49165443 | G | A | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1373-671C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165443 | |||||||
| chr11:49165619 | T | C | 1 | a0001c0010t0002g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1373-847A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165619 | |||||||
| chr11:49165627 | A | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1373-855T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165627 | |||||||
| chr11:49165732 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-960C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165732 | |||||||
| chr11:49165810 | G | T | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1373-1038C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165810 | |||||||
| chr11:49166113 | A | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0237 |
3 | HG03139.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1373-1341T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166113 | |||||||
| chr11:49166155 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-1383G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166155 | |||||||
| chr11:49166292 | G | A | 6 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(3): Show |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-1520C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166292 | |||||||
| chr11:49166495 | G | C | 8 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0291 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1373-1723C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166495 | |||||||
| chr11:49166629 | G | T | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1373-1857C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166629 | |||||||
| chr11:49166634 | G | A | 6 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(3): Show |
7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-1862C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166634 | |||||||
| chr11:49166679 | C | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1373-1907G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166679 | |||||||
| chr11:49166701 | A | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1373-1929T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166701 | |||||||
| chr11:49166745 | T | C | 141 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(138): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1373-1973A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166745 | |||||||
| chr11:49166745 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1373-1973A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166745 | |||||||
| chr11:49166844 | G | C | 1 | a0001c0001t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1373-2072C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166844 | |||||||
| chr11:49166953 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1373-2181C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166953 | |||||||
| chr11:49166975 | G | T | 7 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-2203C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166975 | |||||||
| chr11:49167046 | C | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
20 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1372+2149G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167046 | |||||||
| chr11:49167046 | CAAA | C | 130 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(127): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1372+2146_1372+214 others(7): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167046 | |||||||
| chr11:49167049 | A | C | 10 | a0001c0001t0007g0008 a0003c0005t0002g0029 a0003c0005t0002g0030 others(7): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1372+2146T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167049 | |||||||
| chr11:49167186 | A | G | 8 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(5): Show |
8 | HG02630.hp1 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1372+2009T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167186 | |||||||
| chr11:49167243 | C | G | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1372+1952G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167243 | |||||||
| chr11:49167273 | T | C | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1372+1922A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167273 | |||||||
| chr11:49167343 | A | G | 1 | a0002c0003t0013g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1372+1852T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167343 | |||||||
| chr11:49167437 | T | C | 9 | a0001c0001t0002g0105 a0001c0001t0002g0187 a0001c0001t0002g0188 others(6): Show |
9 | NA18948.hp1 NA18953.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1372+1758A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167437 | |||||||
| chr11:49167471 | C | T | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1372+1724G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167471 | |||||||
| chr11:49167539 | G | A | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1372+1656C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167539 | |||||||
| chr11:49167589 | T | C | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1372+1606A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167589 | |||||||
| chr11:49167615 | G | A | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1372+1580C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167615 | |||||||
| chr11:49167683 | G | A | 93 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(90): Show |
98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1372+1512C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167683 | |||||||
| chr11:49167685 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1372+1510A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167685 | |||||||
| chr11:49167719 | T | C | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+1476A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167719 | |||||||
| chr11:49167865 | A | C | 188 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(185): Show |
218 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1372+1330T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167865 | |||||||
| chr11:49167903 | A | G | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1372+1292T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167903 | |||||||
| chr11:49167923 | C | A | 4 | a0001c0001t0002g0163 a0002c0002t0001g0025 a0002c0002t0001g0300 others(1): Show |
5 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372+1272G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167923 | |||||||
| chr11:49167924 | C | CAGAAAA | 320 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(317): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1372+1265_1372+127 others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167924 | |||||||
| chr11:49167958 | G | A | 1 | a0002c0002t0003g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1372+1237C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167958 | |||||||
| chr11:49168000 | C | G | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1372+1195G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168000 | |||||||
| chr11:49168044 | C | CT | 37 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
42 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1372+1150dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | |||||||
| chr11:49168044 | CT | C | 140 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(137): Show |
168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1372+1150delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | |||||||
| chr11:49168044 | CTT | C | 16 | a0001c0004t0001g0111 a0002c0002t0001g0289 a0002c0002t0001g0290 others(13): Show |
16 | HG01109.hp2 HG01346.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1372+1149_1372+115 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | |||||||
| chr11:49168055 | T | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1372+1140A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168055 | |||||||
| chr11:49168059 | TG | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372+1135delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168059 | |||||||
| chr11:49168074 | A | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0154 |
2 | NA18943.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1372+1121T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168074 | |||||||
| chr11:49168090 | G | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1105C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168090 | |||||||
| chr11:49168092 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1103G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168092 | |||||||
| chr11:49168093 | G | C | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1102C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168093 | |||||||
| chr11:49168095 | TAGGAATC others(62): Show |
T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1031_1372+109 others(73): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168095 | |||||||
| chr11:49168166 | A | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1029T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168166 | |||||||
| chr11:49168167 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1028G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168167 | |||||||
| chr11:49168173 | A | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1022T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168173 | |||||||
| chr11:49168177 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1018G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168177 | |||||||
| chr11:49168182 | TAATGACA others(149): Show |
T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+857_1372+1012 others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168182 | |||||||
| chr11:49168220 | T | C | 1 | a0002c0003t0001g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1372+975A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168220 | |||||||
| chr11:49168231 | C | T | 1 | a0002c0002t0003g0280 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1372+964G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168231 | |||||||
| chr11:49168279 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1372+916A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168279 | |||||||
| chr11:49168379 | T | C | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+816A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168379 | |||||||
| chr11:49168479 | C | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+716G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168479 | |||||||
| chr11:49168600 | A | G | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1372+595T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168600 | |||||||
| chr11:49168691 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | NA18991.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1372+504C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168691 | |||||||
| chr11:49168718 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1372+477C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168718 | |||||||
| chr11:49168740 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1372+455G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168740 | |||||||
| chr11:49168924 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1372+271A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168924 | |||||||
| chr11:49168942 | A | G | 1 | a0002c0002t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1372+253T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168942 | |||||||
| chr11:49169108 | A | G | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+87T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49169108 | |||||||
| chr11:49169308 | T | A | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1309-50A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169308 | |||||||
| chr11:49169309 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1309-51G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169309 | |||||||
| chr11:49169398 | C | G | 1 | a0002c0003t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1309-140G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169398 | |||||||
| chr11:49169439 | C | G | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1309-181G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169439 | |||||||
| chr11:49169611 | C | T | 130 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(127): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1309-353G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169611 | |||||||
| chr11:49169716 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1309-458T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169716 | |||||||
| chr11:49169816 | G | A | 1 | a0002c0002t0003g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1309-558C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169816 | |||||||
| chr11:49169958 | G | T | 2 | a0002c0002t0001g0307 a0002c0002t0001g0317 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1309-700C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169958 | |||||||
| chr11:49170066 | GGTTT | G | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1309-812_1309-809d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170066 | |||||||
| chr11:49170073 | C | A | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1309-815G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170073 | |||||||
| chr11:49170182 | T | G | 1 | a0002c0002t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1309-924A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170182 | |||||||
| chr11:49170332 | C | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+863G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170332 | |||||||
| chr11:49170348 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1308+847G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170348 | |||||||
| chr11:49170359 | A | G | 1 | a0002c0002t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1308+836T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170359 | |||||||
| chr11:49170431 | A | G | 1 | a0001c0001t0002g0214 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1308+764T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170431 | |||||||
| chr11:49170440 | C | A | 1 | a0002c0002t0003g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1308+755G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170440 | |||||||
| chr11:49170476 | G | A | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1308+719C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170476 | |||||||
| chr11:49170540 | G | A | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1308+655C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170540 | |||||||
| chr11:49170672 | G | A | 131 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(128): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1308+523C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170672 | |||||||
| chr11:49170750 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+445T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170750 | |||||||
| chr11:49170799 | G | C | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1308+396C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170799 | |||||||
| chr11:49170974 | T | C | 1 | a0002c0002t0008g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1308+221A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170974 | |||||||
| chr11:49170985 | T | C | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1308+210A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170985 | |||||||
| chr11:49170999 | T | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+196A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170999 | |||||||
| chr11:49171055 | G | T | 1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1308+140C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171055 | |||||||
| chr11:49171075 | T | G | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1308+120A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171075 | |||||||
| chr11:49171115 | C | T | 131 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(128): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1308+80G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171115 | |||||||
| chr11:49171138 | T | C | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1308+57A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171138 | |||||||
| chr11:49171353 | G | GA | 6 | a0001c0004t0001g0112 a0002c0002t0001g0289 a0002c0002t0001g0311 others(3): Show |
6 | HG00544.hp2 HG01346.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-77dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171353 | |||||||
| chr11:49171353 | GA | G | 152 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(149): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1226-77delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171353 | |||||||
| chr11:49171440 | T | C | 1 | a0002c0002t0003g0271 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1226-163A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171440 | |||||||
| chr11:49171535 | T | A | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1226-258A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171535 | |||||||
| chr11:49172150 | T | C | 7 | a0001c0001t0002g0014 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
8 | HG00438.hp1 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1226-873A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172150 | |||||||
| chr11:49172321 | T | C | 2 | a0001c0001t0002g0116 a0001c0001t0002g0200 |
2 | HG01175.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1225+1036A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172321 | |||||||
| chr11:49172395 | CA | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+961delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172395 | |||||||
| chr11:49172638 | G | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+719C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172638 | |||||||
| chr11:49172719 | C | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+638G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172719 | |||||||
| chr11:49172744 | T | A | 35 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(32): Show |
41 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1225+613A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172744 | |||||||
| chr11:49172813 | A | G | 1 | a0002c0002t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225+544T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172813 | |||||||
| chr11:49172827 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1225+530C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172827 | |||||||
| chr11:49172860 | G | A | 1 | a0001c0001t0005g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1225+497C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172860 | |||||||
| chr11:49172918 | G | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+439C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172918 | |||||||
| chr11:49172933 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0174 a0001c0001t0002g0175 |
4 | HG00735.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+424C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172933 | |||||||
| chr11:49172997 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1225+360G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172997 | |||||||
| chr11:49173005 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1225+352G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173005 | |||||||
| chr11:49173082 | A | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+275T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173082 | |||||||
| chr11:49173338 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1225+19A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173338 | |||||||
| chr11:49173342 | G | A | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1225+15C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173342 | |||||||
| chr11:49173345 | T | C | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1225+12A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173345 | |||||||
| chr11:49173538 | T | C | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1106-62A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173538 | |||||||
| chr11:49173575 | C | CA | 134 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(131): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1106-100dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173575 | |||||||
| chr11:49173576 | AG | A | 143 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1106-101delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173576 | |||||||
| chr11:49173577 | G | A | 146 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(143): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1106-101C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173577 | |||||||
| chr11:49173620 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1106-144C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173620 | |||||||
| chr11:49173648 | T | G | 2 | a0001c0001t0002g0127 a0001c0001t0002g0215 |
2 | NA18952.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1106-172A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173648 | |||||||
| chr11:49173666 | A | C | 1 | a0002c0003t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1106-190T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173666 | |||||||
| chr11:49173716 | C | T | 6 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0189 others(3): Show |
6 | NA18948.hp1 NA18953.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-240G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173716 | |||||||
| chr11:49173779 | T | TCC | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1106-304_1106-303i others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173779 | |||||||
| chr11:49173885 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1106-409G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173885 | |||||||
| chr11:49173991 | G | A | 130 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(127): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1106-515C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173991 | |||||||
| chr11:49174204 | T | A | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+688A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174204 | |||||||
| chr11:49174248 | C | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+644G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174248 | |||||||
| chr11:49174250 | G | C | 93 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(90): Show |
98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1105+642C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174250 | |||||||
| chr11:49174369 | T | C | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1105+523A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174369 | |||||||
| chr11:49174426 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105+466A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174426 | |||||||
| chr11:49174576 | A | T | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+316T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174576 | |||||||
| chr11:49174603 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1105+289G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174603 | |||||||
| chr11:49174685 | AC | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+206delG | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174685 | |||||||
| chr11:49174780 | C | CGTTT | 5 | a0002c0003t0001g0035 a0004c0006t0004g0026 a0004c0006t0004g0318 others(2): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105+108_1105+111d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174780 | |||||||
| chr11:49174780 | C | T | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+112G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174780 | |||||||
| chr11:49174781 | G | C | 129 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(126): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1105+111C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174781 | |||||||
| chr11:49175003 | TA | T | 6 | a0001c0001t0002g0100 a0002c0002t0003g0273 a0004c0006t0004g0026 others(3): Show |
7 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-27delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175003 | |||||||
| chr11:49175040 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1020-63C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175040 | |||||||
| chr11:49175100 | C | T | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1020-123G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175100 | |||||||
| chr11:49175233 | G | A | 93 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(90): Show |
98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1020-256C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175233 | |||||||
| chr11:49175334 | CT | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-358delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175334 | |||||||
| chr11:49175353 | C | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1020-376G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175353 | |||||||
| chr11:49175395 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0005 others(88): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1020-418A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175395 | |||||||
| chr11:49175819 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0154 |
2 | NA18943.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1019+40G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175819 | |||||||
| chr11:49175996 | C | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-39G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49175996 | |||||||
| chr11:49176225 | A | T | 1 | a0002c0003t0001g0077 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.921-268T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176225 | |||||||
| chr11:49176528 | T | C | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.921-571A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176528 | |||||||
| chr11:49176807 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-850C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176807 | |||||||
| chr11:49176820 | C | CTG | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.921-864_921-863ins others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176820 | |||||||
| chr11:49176824 | A | AAT | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.921-868_921-867ins others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176824 | |||||||
| chr11:49176825 | C | G | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.921-868G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176825 | |||||||
| chr11:49176912 | G | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-955C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176912 | |||||||
| chr11:49176947 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.921-990G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176947 | |||||||
| chr11:49177049 | C | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.921-1092G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177049 | |||||||
| chr11:49177055 | C | T | 1 | a0002c0003t0001g0051 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.921-1098G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177055 | |||||||
| chr11:49177177 | C | T | 6 | a0002c0003t0001g0004 a0002c0003t0001g0077 a0002c0003t0001g0078 others(3): Show |
8 | NA18944.hp1 NA18945.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.921-1220G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177177 | |||||||
| chr11:49177247 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-1290A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177247 | |||||||
| chr11:49177372 | C | T | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.921-1415G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177372 | |||||||
| chr11:49177428 | T | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-1471A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177428 | |||||||
| chr11:49177622 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-1665G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177622 | |||||||
| chr11:49177721 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.921-1764C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177721 | |||||||
| chr11:49177730 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.921-1773G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177730 | |||||||
| chr11:49177785 | T | TA | 145 | a0001c0001t0001g0027 a0001c0001t0001g0122 a0001c0001t0001g0123 others(142): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.921-1829dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | |||||||
| chr11:49177785 | T | TAA | 7 | a0001c0001t0002g0098 a0001c0001t0002g0103 a0001c0001t0002g0154 others(4): Show |
7 | HG02523.hp1 HG04115.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-1830_921-1829d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | |||||||
| chr11:49177785 | TA | T | 10 | a0001c0001t0001g0221 a0001c0001t0016g0325 a0002c0002t0001g0308 others(7): Show |
10 | HG00609.hp2 HG01346.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.921-1829delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | |||||||
| chr11:49177894 | T | C | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-1937A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177894 | |||||||
| chr11:49177895 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.921-1938T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177895 | |||||||
| chr11:49177963 | CA | C | 278 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(275): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.921-2007delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177963 | |||||||
| chr11:49178036 | G | C | 324 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(321): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.921-2079C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178036 | |||||||
| chr11:49178083 | C | T | 1 | a0002c0002t0001g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.921-2126G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178083 | |||||||
| chr11:49178111 | G | T | 155 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(152): Show |
180 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.921-2154C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178111 | |||||||
| chr11:49178196 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-2239T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178196 | |||||||
| chr11:49178231 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.921-2274A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178231 | |||||||
| chr11:49178497 | G | A | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.921-2540C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178497 | |||||||
| chr11:49178660 | C | A | 1 | a0001c0004t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.921-2703G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178660 | |||||||
| chr11:49178775 | G | A | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.921-2818C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178775 | |||||||
| chr11:49178820 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.921-2863G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178820 | |||||||
| chr11:49178840 | T | G | 1 | a0002c0003t0001g0043 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.921-2883A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178840 | |||||||
| chr11:49179065 | A | G | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | NA18951.hp1 NA18964.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-3108T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179065 | |||||||
| chr11:49179269 | G | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-3312C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179269 | |||||||
| chr11:49179329 | C | T | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.921-3372G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179329 | |||||||
| chr11:49179398 | T | G | 1 | a0002c0002t0001g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.921-3441A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179398 | |||||||
| chr11:49179517 | G | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3560C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179517 | |||||||
| chr11:49179594 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.920+3555A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179594 | |||||||
| chr11:49179626 | T | C | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+3523A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179626 | |||||||
| chr11:49179759 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.920+3390A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179759 | |||||||
| chr11:49179810 | C | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+3339G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179810 | |||||||
| chr11:49179819 | C | T | 151 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(148): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.920+3330G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179819 | |||||||
| chr11:49179882 | T | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0316 |
3 | HG02896.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.920+3267A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179882 | |||||||
| chr11:49179914 | A | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0203 |
3 | NA18960.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.920+3235T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179914 | |||||||
| chr11:49180061 | C | T | 136 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(133): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.920+3088G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180061 | |||||||
| chr11:49180062 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+3087C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180062 | |||||||
| chr11:49180088 | T | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+3061A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180088 | |||||||
| chr11:49180116 | C | G | 155 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(152): Show |
180 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.920+3033G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180116 | |||||||
| chr11:49180128 | C | T | 149 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(146): Show |
173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.920+3021G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180128 | |||||||
| chr11:49180142 | A | ACTCT | 5 | a0003c0005t0002g0029 a0003c0005t0002g0030 a0003c0005t0006g0028 others(2): Show |
6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+3003_920+3006d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180142 | |||||||
| chr11:49180264 | C | A | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.920+2885G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180264 | |||||||
| chr11:49180289 | C | T | 5 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(2): Show |
5 | HG00544.hp1 HG02300.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+2860G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180289 | |||||||
| chr11:49180352 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+2797T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180352 | |||||||
| chr11:49180491 | C | A | 1 | a0001c0001t0002g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.920+2658G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180491 | |||||||
| chr11:49180503 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.920+2646T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180503 | |||||||
| chr11:49180611 | T | C | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+2538A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180611 | |||||||
| chr11:49180635 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+2514C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180635 | |||||||
| chr11:49180642 | A | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.920+2507T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180642 | |||||||
| chr11:49180835 | A | G | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+2314T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180835 | |||||||
| chr11:49180874 | C | T | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.920+2275G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180874 | |||||||
| chr11:49180889 | T | C | 1 | a0002c0002t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.920+2260A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180889 | |||||||
| chr11:49181017 | G | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.920+2132C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181017 | |||||||
| chr11:49181107 | A | AT | 15 | a0001c0001t0001g0229 a0001c0001t0001g0232 a0002c0002t0001g0245 others(12): Show |
15 | HG02145.hp1 HG02300.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.920+2041dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181107 | |||||||
| chr11:49181107 | AT | A | 140 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(137): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.920+2041delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181107 | |||||||
| chr11:49181139 | A | T | 1 | a0001c0001t0002g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920+2010T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181139 | |||||||
| chr11:49181203 | G | T | 1 | a0002c0003t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.920+1946C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181203 | |||||||
| chr11:49181271 | C | A | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920+1878G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181271 | |||||||
| chr11:49181333 | A | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1816T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181333 | |||||||
| chr11:49181448 | A | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1701T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181448 | |||||||
| chr11:49181534 | T | C | 3 | a0004c0006t0004g0318 a0004c0006t0004g0319 a0004c0006t0004g0320 |
3 | HG02615.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.920+1615A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181534 | |||||||
| chr11:49181762 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1387T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181762 | |||||||
| chr11:49181783 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1366G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181783 | |||||||
| chr11:49181935 | A | G | 82 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(79): Show |
87 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.920+1214T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181935 | |||||||
| chr11:49182055 | G | A | 1 | a0002c0003t0001g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.920+1094C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182055 | |||||||
| chr11:49182061 | C | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.920+1088G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182061 | |||||||
| chr11:49182115 | G | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1034C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182115 | |||||||
| chr11:49182150 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+999C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182150 | |||||||
| chr11:49182253 | C | T | 12 | a0001c0004t0001g0102 a0001c0004t0001g0108 a0001c0004t0001g0109 others(9): Show |
13 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.920+896G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182253 | |||||||
| chr11:49182254 | A | G | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.920+895T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182254 | |||||||
| chr11:49182310 | C | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+839G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182310 | |||||||
| chr11:49182328 | C | CA | 73 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(70): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.920+820dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | |||||||
| chr11:49182328 | C | CAA | 84 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0227 others(81): Show |
91 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.920+819_920+820dup others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | |||||||
| chr11:49182328 | C | CAAA | 120 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(117): Show |
133 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.920+818_920+820dup others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | |||||||
| chr11:49182328 | C | CAAAA | 41 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0092 others(38): Show |
44 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.920+817_920+820dup others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | |||||||
| chr11:49182358 | G | A | 1 | a0002c0003t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.920+791C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182358 | |||||||
| chr11:49182514 | C | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+635G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182514 | |||||||
| chr11:49182524 | G | C | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+625C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182524 | |||||||
| chr11:49182545 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.920+604G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182545 | |||||||
| chr11:49182565 | C | T | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.920+584G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182565 | |||||||
| chr11:49182584 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0177 |
2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.920+565T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182584 | |||||||
| chr11:49182633 | A | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+516T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182633 | |||||||
| chr11:49182862 | A | C | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.920+287T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182862 | |||||||
| chr11:49182863 | A | T | 144 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(141): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.920+286T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182863 | |||||||
| chr11:49182892 | C | T | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.920+257G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182892 | |||||||
| chr11:49183017 | A | G | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+132T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49183017 | |||||||
| chr11:49183293 | C | T | 3 | a0002c0003t0001g0084 a0002c0003t0001g0085 a0002c0003t0001g0086 |
3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.827-51G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183293 | |||||||
| chr11:49183412 | A | T | 5 | a0002c0002t0002g0268 a0002c0002t0003g0022 a0002c0002t0003g0261 others(2): Show |
6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-170T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183412 | |||||||
| chr11:49183569 | G | A | 139 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(136): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.827-327C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183569 | |||||||
| chr11:49183578 | A | G | 1 | a0002c0002t0003g0272 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.827-336T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183578 | |||||||
| chr11:49183661 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.827-419G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183661 | |||||||
| chr11:49183709 | C | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827-467G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183709 | |||||||
| chr11:49183851 | G | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-609C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183851 | |||||||
| chr11:49183986 | A | G | 2 | a0002c0003t0001g0033 a0002c0003t0001g0034 |
2 | HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.827-744T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183986 | |||||||
| chr11:49184082 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827-840A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184082 | |||||||
| chr11:49184167 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.827-925A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184167 | |||||||
| chr11:49184275 | A | G | 1 | a0002c0003t0002g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.827-1033T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184275 | |||||||
| chr11:49184305 | A | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-1063T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184305 | |||||||
| chr11:49184386 | T | C | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.827-1144A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184386 | |||||||
| chr11:49184439 | T | G | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1197A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184439 | |||||||
| chr11:49184588 | T | A | 1 | a0001c0001t0002g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.826+1081A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184588 | |||||||
| chr11:49184678 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.826+991G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184678 | |||||||
| chr11:49184773 | A | C | 138 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(135): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.826+896T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184773 | |||||||
| chr11:49184937 | A | G | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.826+732T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184937 | |||||||
| chr11:49185173 | C | T | 1 | a0002c0002t0001g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.826+496G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185173 | |||||||
| chr11:49185305 | G | T | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.826+364C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185305 | |||||||
| chr11:49185326 | G | A | 1 | a0002c0002t0003g0278 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.826+343C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185326 | |||||||
| chr11:49185364 | A | G | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.826+305T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185364 | |||||||
| chr11:49185525 | A | C | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.826+144T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185525 | |||||||
| chr11:49185580 | T | C | 1 | a0002c0002t0003g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.826+89A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185580 | |||||||
| chr11:49185909 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.640-54C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49185909 | |||||||
| chr11:49185942 | A | G | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.640-87T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49185942 | |||||||
| chr11:49186155 | T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.640-300A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186155 | |||||||
| chr11:49186224 | A | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-369T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186224 | |||||||
| chr11:49186267 | T | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+377A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186267 | |||||||
| chr11:49186347 | A | G | 1 | a0001c0001t0002g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.639+297T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186347 | |||||||
| chr11:49186478 | C | G | 1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639+166G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186478 | |||||||
| chr11:49186617 | G | GA | 9 | a0002c0002t0003g0023 a0002c0002t0003g0269 a0002c0002t0003g0270 others(6): Show |
10 | HG00558.hp2 HG02040.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.639+26dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186617 | |||||||
| chr11:49186626 | A | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+18T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186626 | |||||||
| chr11:49186827 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-58C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49186827 | |||||||
| chr11:49186962 | A | G | 1 | a0002c0003t0001g0031 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.514-193T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49186962 | |||||||
| chr11:49187031 | A | C | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.514-262T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187031 | |||||||
| chr11:49187041 | C | G | 4 | a0002c0002t0003g0023 a0002c0002t0003g0269 a0002c0002t0003g0270 others(1): Show |
5 | HG02040.hp2 NA18944.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-272G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187041 | |||||||
| chr11:49187043 | CA | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
28 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.514-275delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187043 | |||||||
| chr11:49187044 | A | C | 2 | a0001c0001t0001g0242 a0002c0003t0001g0060 |
2 | HG02165.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.514-275T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187044 | |||||||
| chr11:49187086 | G | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.514-317C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187086 | |||||||
| chr11:49187097 | G | C | 1 | a0002c0002t0003g0282 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.514-328C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187097 | |||||||
| chr11:49187165 | G | T | 2 | a0003c0005t0002g0029 a0003c0005t0002g0030 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.514-396C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187165 | |||||||
| chr11:49187197 | T | C | 2 | a0001c0001t0002g0098 a0001c0001t0002g0178 |
2 | NA18940.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.514-428A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187197 | |||||||
| chr11:49187225 | G | T | 1 | a0002c0003t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.514-456C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187225 | |||||||
| chr11:49187232 | A | C | 1 | a0002c0002t0001g0305 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.514-463T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187232 | |||||||
| chr11:49187310 | G | T | 138 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(135): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.514-541C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187310 | |||||||
| chr11:49187316 | C | T | 138 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(135): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.514-547G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187316 | |||||||
| chr11:49187383 | C | A | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.514-614G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187383 | |||||||
| chr11:49187395 | A | G | 1 | a0002c0003t0001g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.514-626T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187395 | |||||||
| chr11:49187511 | T | G | 321 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(318): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.514-742A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187511 | |||||||
| chr11:49187713 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514-944T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187713 | |||||||
| chr11:49187745 | G | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-976C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187745 | |||||||
| chr11:49187786 | T | C | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1017A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187786 | |||||||
| chr11:49187900 | T | C | 1 | a0002c0003t0001g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.514-1131A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187900 | |||||||
| chr11:49187936 | T | C | 4 | a0002c0003t0001g0058 a0002c0003t0001g0059 a0002c0003t0001g0074 others(1): Show |
4 | HG03704.hp2 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1167A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187936 | |||||||
| chr11:49188019 | T | C | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.514-1250A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188019 | |||||||
| chr11:49188051 | C | G | 5 | a0002c0002t0002g0268 a0002c0002t0003g0022 a0002c0002t0003g0261 others(2): Show |
6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1282G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188051 | |||||||
| chr11:49188096 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.514-1327C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188096 | |||||||
| chr11:49188170 | A | T | 140 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(137): Show |
164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.514-1401T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188170 | |||||||
| chr11:49188202 | G | T | 1 | a0002c0003t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.514-1433C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188202 | |||||||
| chr11:49188208 | G | A | 1 | a0002c0003t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.514-1439C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188208 | |||||||
| chr11:49188282 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.514-1513C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188282 | |||||||
| chr11:49188390 | T | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1621A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188390 | |||||||
| chr11:49188391 | G | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1622C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188391 | |||||||
| chr11:49188487 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-1718G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188487 | |||||||
| chr11:49188512 | C | CA | 221 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0322 others(218): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.514-1744dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188512 | |||||||
| chr11:49188512 | C | CAA | 56 | a0001c0001t0002g0194 a0001c0001t0002g0205 a0001c0001t0014g0180 others(53): Show |
74 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.514-1745_514-1744d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188512 | |||||||
| chr11:49188642 | G | T | 291 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(288): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.514-1873C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188642 | |||||||
| chr11:49188667 | C | T | 2 | a0003c0005t0002g0029 a0003c0005t0002g0030 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.514-1898G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188667 | |||||||
| chr11:49188695 | T | A | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.514-1926A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188695 | |||||||
| chr11:49188972 | A | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.514-2203T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188972 | |||||||
| chr11:49189003 | T | C | 4 | a0002c0002t0003g0021 a0002c0002t0003g0247 a0002c0002t0003g0248 others(1): Show |
5 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2234A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189003 | |||||||
| chr11:49189042 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.514-2273G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189042 | |||||||
| chr11:49189155 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.514-2386G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189155 | |||||||
| chr11:49189186 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-2417G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189186 | |||||||
| chr11:49189538 | C | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2769G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189538 | |||||||
| chr11:49189645 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-2876C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189645 | |||||||
| chr11:49189676 | T | C | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.514-2907A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189676 | |||||||
| chr11:49189998 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.513+2795G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189998 | |||||||
| chr11:49190000 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+2793G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190000 | |||||||
| chr11:49190252 | A | G | 279 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0002 others(276): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.513+2541T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190252 | |||||||
| chr11:49190313 | A | C | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+2480T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190313 | |||||||
| chr11:49190704 | T | C | 3 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0012g0184 |
3 | HG03942.hp2 NA18952.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.513+2089A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190704 | |||||||
| chr11:49191106 | C | G | 1 | a0002c0002t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.513+1687G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191106 | |||||||
| chr11:49191135 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+1658G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191135 | |||||||
| chr11:49191140 | T | C | 1 | a0004c0006t0004g0320 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+1653A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191140 | |||||||
| chr11:49191147 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
5 | HG01515.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1646C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191147 | |||||||
| chr11:49191375 | C | T | 4 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1418G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191375 | |||||||
| chr11:49191410 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.513+1383T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191410 | |||||||
| chr11:49191456 | A | C | 1 | a0004c0006t0004g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513+1337T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191456 | |||||||
| chr11:49191650 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+1143C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191650 | |||||||
| chr11:49191694 | T | C | 1 | a0002c0002t0004g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.513+1099A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191694 | |||||||
| chr11:49191729 | G | A | 5 | a0002c0003t0001g0061 a0002c0003t0001g0062 a0002c0003t0001g0063 others(2): Show |
5 | HG00099.hp2 HG01433.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1064C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191729 | |||||||
| chr11:49191735 | TCA | T | 138 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(135): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.513+1056_513+1057d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191735 | |||||||
| chr11:49191793 | G | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1000C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191793 | |||||||
| chr11:49191935 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+858C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191935 | |||||||
| chr11:49191952 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(30): Show |
37 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.513+841G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191952 | |||||||
| chr11:49192294 | G | T | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.513+499C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192294 | |||||||
| chr11:49192325 | T | C | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+468A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192325 | |||||||
| chr11:49192354 | G | A | 4 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+439C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192354 | |||||||
| chr11:49192411 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513+382A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192411 | |||||||
| chr11:49192496 | C | A | 186 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(183): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.513+297G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192496 | |||||||
| chr11:49192692 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.513+101A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192692 | |||||||
| chr11:49192947 | G | A | 186 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(183): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.412-53C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49192947 | |||||||
| chr11:49192980 | T | A | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.412-86A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49192980 | |||||||
| chr11:49193016 | T | G | 9 | a0001c0001t0002g0105 a0001c0001t0002g0187 a0001c0001t0002g0188 others(6): Show |
9 | NA18948.hp1 NA18953.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-122A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193016 | |||||||
| chr11:49193464 | C | T | 61 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0013 others(58): Show |
66 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.412-570G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193464 | |||||||
| chr11:49193482 | A | G | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.412-588T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193482 | |||||||
| chr11:49193552 | C | A | 4 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-658G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193552 | |||||||
| chr11:49193681 | A | C | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-787T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193681 | |||||||
| chr11:49193736 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-842G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193736 | |||||||
| chr11:49193738 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.412-844T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193738 | |||||||
| chr11:49193879 | G | A | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.412-985C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193879 | |||||||
| chr11:49193936 | G | A | 1 | a0005c0007t0009g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.412-1042C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193936 | |||||||
| chr11:49193962 | A | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-1068T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193962 | |||||||
| chr11:49193987 | G | A | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-1093C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193987 | |||||||
| chr11:49194003 | C | G | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.412-1109G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194003 | |||||||
| chr11:49194078 | G | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.412-1184C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194078 | |||||||
| chr11:49194081 | G | T | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.412-1187C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194081 | |||||||
| chr11:49194083 | C | T | 85 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(82): Show |
90 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.412-1189G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194083 | |||||||
| chr11:49194087 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-1193G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194087 | |||||||
| chr11:49194132 | C | CA | 100 | a0001c0001t0001g0237 a0001c0001t0002g0099 a0001c0001t0002g0105 others(97): Show |
107 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.412-1239dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | |||||||
| chr11:49194132 | C | CAA | 10 | a0002c0002t0001g0296 a0002c0002t0001g0315 a0002c0003t0001g0040 others(7): Show |
10 | HG00621.hp2 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.412-1240_412-1239d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | |||||||
| chr11:49194132 | CA | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0218 a0001c0001t0001g0219 others(8): Show |
13 | HG01192.hp1 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-1239delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | |||||||
| chr11:49194238 | A | G | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-1344T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194238 | |||||||
| chr11:49194296 | T | C | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-1402A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194296 | |||||||
| chr11:49194316 | A | C | 1 | a0003c0005t0006g0326 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.412-1422T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194316 | |||||||
| chr11:49194405 | T | A | 1 | a0001c0001t0002g0206 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.412-1511A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194405 | |||||||
| chr11:49194538 | A | C | 3 | a0001c0001t0002g0095 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02280.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-1644T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194538 | |||||||
| chr11:49194604 | G | A | 2 | a0002c0002t0003g0256 a0002c0002t0003g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412-1710C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194604 | |||||||
| chr11:49194702 | G | T | 1 | a0001c0001t0002g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.412-1808C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194702 | |||||||
| chr11:49194869 | A | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-1975T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194869 | |||||||
| chr11:49194962 | G | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-2068C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194962 | |||||||
| chr11:49195019 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-2125G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195019 | |||||||
| chr11:49195028 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.412-2134A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195028 | |||||||
| chr11:49195059 | C | G | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2165G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195059 | |||||||
| chr11:49195147 | C | T | 147 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(144): Show |
172 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.412-2253G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195147 | |||||||
| chr11:49195249 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.412-2355C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195249 | |||||||
| chr11:49195454 | A | G | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.412-2560T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195454 | |||||||
| chr11:49195581 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-2687T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195581 | |||||||
| chr11:49195614 | A | C | 56 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 others(53): Show |
75 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.412-2720T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195614 | |||||||
| chr11:49195675 | GA | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.412-2782delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195675 | |||||||
| chr11:49195759 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2865T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195759 | |||||||
| chr11:49195817 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412-2923T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195817 | |||||||
| chr11:49195840 | A | C | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG02965.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-2946T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195840 | |||||||
| chr11:49196010 | C | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-3116G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196010 | |||||||
| chr11:49196013 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-3119C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196013 | |||||||
| chr11:49196062 | G | A | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.412-3168C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196062 | |||||||
| chr11:49196068 | T | G | 58 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 others(55): Show |
77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.412-3174A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196068 | |||||||
| chr11:49196282 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.412-3388C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196282 | |||||||
| chr11:49196320 | G | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-3426C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196320 | |||||||
| chr11:49196362 | A | G | 1 | a0002c0003t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-3468T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196362 | |||||||
| chr11:49196625 | A | AT | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+3629_411+3630i others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196625 | |||||||
| chr11:49196661 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.411+3594G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196661 | |||||||
| chr11:49196662 | G | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+3593C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196662 | |||||||
| chr11:49196694 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.411+3561T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196694 | |||||||
| chr11:49196827 | A | G | 1 | a0002c0002t0003g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411+3428T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196827 | |||||||
| chr11:49196874 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.411+3381A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196874 | |||||||
| chr11:49196892 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.411+3363C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196892 | |||||||
| chr11:49197011 | A | G | 1 | a0002c0002t0001g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.411+3244T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197011 | |||||||
| chr11:49197035 | C | T | 1 | a0002c0003t0013g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.411+3220G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197035 | |||||||
| chr11:49197167 | A | G | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+3088T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197167 | |||||||
| chr11:49197307 | T | C | 61 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0013 others(58): Show |
66 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.411+2948A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197307 | |||||||
| chr11:49197551 | T | C | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.411+2704A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197551 | |||||||
| chr11:49197876 | T | C | 4 | a0002c0003t0001g0068 a0002c0003t0001g0069 a0002c0003t0001g0070 others(1): Show |
4 | HG01361.hp1 HG01952.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2379A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197876 | |||||||
| chr11:49198173 | C | G | 186 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(183): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.411+2082G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198173 | |||||||
| chr11:49198179 | A | G | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+2076T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198179 | |||||||
| chr11:49198246 | C | A | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+2009G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198246 | |||||||
| chr11:49198373 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.411+1882A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198373 | |||||||
| chr11:49198374 | A | C | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+1881T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198374 | |||||||
| chr11:49198400 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.411+1855A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198400 | |||||||
| chr11:49198407 | G | A | 5 | a0002c0002t0002g0268 a0002c0002t0003g0022 a0002c0002t0003g0261 others(2): Show |
6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+1848C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198407 | |||||||
| chr11:49198435 | T | C | 1 | a0002c0003t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.411+1820A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198435 | |||||||
| chr11:49198440 | C | CCACTGCA others(15): Show |
4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1793_411+1814d others(24): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198440 | |||||||
| chr11:49198481 | C | CA | 135 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0290 others(132): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.411+1773dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198481 | |||||||
| chr11:49198481 | C | CAA | 8 | a0002c0002t0001g0289 a0002c0002t0001g0303 a0002c0002t0003g0286 others(5): Show |
8 | HG01433.hp1 HG02280.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+1772_411+1773d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198481 | |||||||
| chr11:49198490 | C | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+1765G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198490 | |||||||
| chr11:49198542 | T | C | 1 | a0002c0002t0003g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.411+1713A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198542 | |||||||
| chr11:49198687 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
14 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+1568G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198687 | |||||||
| chr11:49198740 | A | G | 1 | a0001c0004t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.411+1515T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198740 | |||||||
| chr11:49198801 | G | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+1454C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198801 | |||||||
| chr11:49198921 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02015.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.411+1334A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198921 | |||||||
| chr11:49198960 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1295T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198960 | |||||||
| chr11:49199037 | C | T | 1 | a0002c0003t0001g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+1218G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199037 | |||||||
| chr11:49199038 | A | G | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+1217T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199038 | |||||||
| chr11:49199057 | G | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.411+1198C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199057 | |||||||
| chr11:49199185 | A | G | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1070T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199185 | |||||||
| chr11:49199271 | G | A | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.411+984C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199271 | |||||||
| chr11:49199315 | T | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+940A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199315 | |||||||
| chr11:49199503 | G | C | 25 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.411+752C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199503 | |||||||
| chr11:49199544 | C | T | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.411+711G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199544 | |||||||
| chr11:49199662 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.411+593G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199662 | |||||||
| chr11:49199689 | T | A | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+566A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199689 | |||||||
| chr11:49199708 | C | T | 2 | a0005c0007t0009g0243 a0005c0007t0009g0244 |
2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+547G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199708 | |||||||
| chr11:49199839 | A | C | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+416T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199839 | |||||||
| chr11:49199860 | G | A | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.411+395C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199860 | |||||||
| chr11:49199936 | T | C | 54 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(51): Show |
72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.411+319A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199936 | |||||||
| chr11:49200233 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.411+22A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49200233 | |||||||
| chr11:49201197 | GT | G | 53 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(50): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.225-757delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201197 | |||||||
| chr11:49201255 | G | GAT | 85 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(82): Show |
90 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.225-816_225-815dup others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATAT | 72 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(69): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.225-818_225-815dup others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATATAT | 12 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0001g0245 others(9): Show |
13 | HG01496.hp1 HG01943.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.225-820_225-815dup others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATATATA others(1): Show |
9 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(6): Show |
9 | NA18942.hp2 NA18964.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-822_225-815dup others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATATATA others(3): Show |
3 | a0002c0002t0003g0261 a0004c0006t0004g0319 a0004c0006t0004g0320 |
3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.225-824_225-815dup others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATATATA others(5): Show |
1 | a0004c0006t0004g0318 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.225-826_225-815dup others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201255 | G | GATATATA others(7): Show |
1 | a0004c0006t0004g0026 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.225-828_225-815dup others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | |||||||
| chr11:49201282 | C | A | 1 | a0002c0002t0003g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225-841G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201282 | |||||||
| chr11:49201284 | T | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-843A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201284 | |||||||
| chr11:49201354 | T | C | 11 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0291 others(8): Show |
11 | HG01109.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-913A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201354 | |||||||
| chr11:49201384 | C | T | 18 | a0002c0002t0003g0010 a0002c0002t0003g0021 a0002c0002t0003g0247 others(15): Show |
21 | HG01243.hp1 HG01257.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.225-943G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201384 | |||||||
| chr11:49201433 | AT | A | 43 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0011 others(40): Show |
60 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.225-993delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201433 | |||||||
| chr11:49201739 | A | G | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG02965.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-1298T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201739 | |||||||
| chr11:49202011 | A | C | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.225-1570T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202011 | |||||||
| chr11:49202534 | G | T | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.225-2093C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202534 | |||||||
| chr11:49202679 | G | A | 181 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(178): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.225-2238C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202679 | |||||||
| chr11:49202689 | C | T | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.225-2248G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202689 | |||||||
| chr11:49202704 | T | G | 2 | a0001c0001t0001g0323 a0001c0001t0015g0324 |
2 | HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-2263A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202704 | |||||||
| chr11:49203135 | ATATTCAA others(13): Show |
A | 1 | a0002c0002t0003g0288 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.225-2714_225-2695d others(22): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203135 | |||||||
| chr11:49203333 | G | A | 1 | a0001c0010t0002g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.224+2734C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203333 | |||||||
| chr11:49203543 | T | A | 1 | a0001c0001t0002g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.224+2524A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203543 | |||||||
| chr11:49203617 | C | T | 3 | a0001c0001t0005g0096 a0001c0001t0005g0097 a0001c0001t0005g0212 |
3 | HG00099.hp1 HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.224+2450G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203617 | |||||||
| chr11:49203699 | G | A | 2 | a0002c0003t0001g0042 a0002c0003t0001g0043 |
2 | NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.224+2368C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203699 | |||||||
| chr11:49203764 | T | A | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+2303A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203764 | |||||||
| chr11:49203800 | G | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+2267C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203800 | |||||||
| chr11:49203832 | C | G | 1 | a0002c0002t0008g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.224+2235G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203832 | |||||||
| chr11:49203974 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224+2093T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203974 | |||||||
| chr11:49204006 | G | T | 1 | a0002c0002t0003g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.224+2061C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204006 | |||||||
| chr11:49204227 | A | T | 17 | a0002c0002t0003g0010 a0002c0002t0003g0021 a0002c0002t0003g0247 others(14): Show |
20 | HG01243.hp1 HG01257.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.224+1840T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204227 | |||||||
| chr11:49204261 | C | T | 3 | a0002c0002t0001g0305 a0002c0002t0001g0306 a0002c0011t0001g0312 |
3 | HG01109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.224+1806G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204261 | |||||||
| chr11:49204336 | T | C | 1 | a0001c0001t0005g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224+1731A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204336 | |||||||
| chr11:49204610 | C | T | 54 | a0002c0002t0002g0268 a0002c0002t0003g0001 a0002c0002t0003g0010 others(51): Show |
72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.224+1457G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204610 | |||||||
| chr11:49204632 | A | G | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.224+1435T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204632 | |||||||
| chr11:49204636 | C | T | 3 | a0003c0005t0006g0028 a0003c0005t0006g0326 a0003c0005t0006g0327 |
4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+1431G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204636 | |||||||
| chr11:49204745 | T | A | 3 | a0002c0003t0001g0084 a0002c0003t0001g0085 a0002c0003t0001g0086 |
3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.224+1322A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204745 | |||||||
| chr11:49205076 | G | T | 1 | a0004c0006t0004g0026 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.224+991C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205076 | |||||||
| chr11:49205131 | G | A | 3 | a0002c0002t0003g0297 a0002c0002t0003g0298 a0002c0002t0003g0299 |
3 | HG02451.hp2 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.224+936C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205131 | |||||||
| chr11:49205164 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.224+903T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205164 | |||||||
| chr11:49205294 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.224+773C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205294 | |||||||
| chr11:49205333 | C | T | 5 | a0003c0005t0002g0029 a0003c0005t0002g0030 a0003c0005t0006g0028 others(2): Show |
6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+734G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205333 | |||||||
| chr11:49205557 | G | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.224+510C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205557 | |||||||
| chr11:49205936 | G | A | 143 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(140): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.224+131C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205936 | |||||||
| chr11:49206018 | T | A | 2 | a0001c0001t0002g0214 a0001c0008t0002g0213 |
2 | HG01168.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224+49A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49206018 | |||||||
| chr11:49206332 | A | C | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.119-160T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206332 | |||||||
| chr11:49206394 | C | T | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-222G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206394 | |||||||
| chr11:49206500 | T | C | 3 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0004g0313 |
3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.119-328A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206500 | |||||||
| chr11:49206505 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.119-333A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206505 | |||||||
| chr11:49206555 | A | G | 6 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(3): Show |
6 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-383T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206555 | |||||||
| chr11:49206572 | CAAAT | C | 3 | a0002c0002t0001g0025 a0002c0002t0001g0300 a0002c0002t0001g0316 |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-404_119-401del others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206572 | |||||||
| chr11:49206835 | T | C | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-663A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206835 | |||||||
| chr11:49207061 | C | G | 147 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(144): Show |
172 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.119-889G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207061 | |||||||
| chr11:49207252 | A | G | 1 | a0002c0002t0003g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.118+1040T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207252 | |||||||
| chr11:49207449 | G | A | 141 | a0002c0002t0001g0025 a0002c0002t0001g0245 a0002c0002t0001g0289 others(138): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.118+843C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207449 | |||||||
| chr11:49207678 | C | A | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.118+614G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207678 | |||||||
| chr11:49207688 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.118+604C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207688 | |||||||
| chr11:49207883 | C | G | 1 | a0005c0007t0009g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.118+409G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207883 | |||||||
| chr11:49207932 | T | TA | 4 | a0004c0006t0004g0026 a0004c0006t0004g0318 a0004c0006t0004g0319 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+359dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207932 | |||||||
| chr11:49207933 | A | T | 4 | a0002c0002t0001g0245 a0002c0002t0001g0301 a0002c0002t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+359T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207933 | |||||||
| chr11:49207936 | AAAAC | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
39 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.118+352_118+355del others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207936 | |||||||
| chr11:49207948 | C | CAAACA | 15 | a0002c0003t0001g0031 a0002c0003t0001g0032 a0002c0003t0001g0033 others(12): Show |
15 | HG01071.hp1 HG01346.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.118+339_118+343dup others(5): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | |||||||
| chr11:49207948 | C | CAAACAAA others(3): Show |
110 | a0002c0002t0001g0245 a0002c0002t0001g0289 a0002c0002t0001g0290 others(107): Show |
133 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.118+334_118+343dup others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | |||||||
| chr11:49207948 | C | CAAACAAA others(8): Show |
17 | a0002c0002t0001g0025 a0002c0002t0001g0301 a0002c0002t0001g0302 others(14): Show |
18 | HG01109.hp2 HG01257.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.118+329_118+343dup others(15): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | |||||||
| chr11:49207948 | C | CAAACAAA others(13): Show |
1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.118+324_118+343dup others(20): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | |||||||
| chr11:49207978 | C | CA | 6 | a0001c0001t0015g0324 a0002c0003t0001g0087 a0004c0006t0004g0026 others(3): Show |
7 | HG01515.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+313dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207978 | |||||||
| chr11:49208226 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+66C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49208226 | |||||||
| chr11:49208281 | C | G | 60 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0013 others(57): Show |
65 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.118+11G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49208281 |