Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2252 |
| ensemblid | ENSG00000140285.12 |
| hgncid | 3685 |
| symbol | FGF7 |
| name | fibroblast growth factor 7 |
| refseq_nuc | NM_002009.4 |
| refseq_prot | NP_002000.1 |
| ensembl_nuc | ENST00000267843.9 |
| ensembl_prot | ENSP00000267843.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 49423242 |
| end | 49488775 |
| strand | + |
| ver | v1.2 |
| region | chr15:49423242-49488775 |
| region5000 | chr15:49418242-49493775 |
| regionname0 | FGF7_chr15_49423242_49488775 |
| regionname5000 | FGF7_chr15_49418242_49493775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 582 | 358 | 86 | 54 | 152 | 14 | 50 | FGF7_chr15_49418242_49493775 | FGF7 | ATGCA others(577): Show |
chr15 | 49418242 | 49493775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5321 | 81 | 34 | 11 | 26 | 4 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0002 | 0/0 | 5317 | 72 | 2 | 17 | 39 | 2 | 12 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5312): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0003 | 0/0 | 5321 | 38 | 1 | 2 | 33 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0004 | 0/1 | 5321 | 30 | 3 | 10 | 2 | 4 | 10 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0005 | 0/0 | 5321 | 23 | 1 | 6 | 15 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0006 | 0/0 | 5321 | 21 | 0 | 1 | 15 | 0 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0007 | 0/0 | 5318 | 15 | 13 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5313): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0008 | 0/0 | 5321 | 13 | 0 | 1 | 9 | 0 | 3 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0009 | 0/0 | 5321 | 11 | 11 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0010 | 0/0 | 5321 | 10 | 1 | 1 | 2 | 1 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0011 | 0/0 | 5318 | 7 | 1 | 0 | 6 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5313): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0012 | 0/0 | 5321 | 5 | 4 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0013 | 0/0 | 5323 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5318): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0014 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0015 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0016 | 0/0 | 5318 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5313): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0017 | 0/0 | 5321 | 3 | 0 | 1 | 0 | 1 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0018 | 0/0 | 5321 | 2 | 0 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0019 | 0/0 | 5321 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0020 | 0/0 | 5320 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5315): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0021 | 0/0 | 5317 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5312): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0022 | 0/0 | 5317 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5312): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0023 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0024 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0025 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0026 | 0/0 | 5321 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0027 | 0/0 | 5317 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5312): Show |
chr15 | 49418242 | 49493775 |
| a0001c0001t0028 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | ACACA others(5316): Show |
chr15 | 49418242 | 49493775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 1 | 1 | 4 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 4 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0011 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0008 | 0/0 | 5 | 0 | 0 | 0 | 3 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0011g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0011g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0012g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0013g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0015g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0015g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0016g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0017g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0017g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0018g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0019g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0020g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0020g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0021g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0023g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0024g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0025g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0026g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0027g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| a0001c0001t0028g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | GBR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | GBR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0232 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00558 | hp1 | a0001 | c0001 | t0016 | g0069 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0237 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0226 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0080 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0048 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01192 | hp2 | a0001 | c0001 | t0017 | g0001 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0015 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0236 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01257 | hp1 | a0001 | c0001 | t0021 | g0210 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01516 | hp2 | a0001 | c0001 | t0019 | g0032 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01517 | hp1 | a0001 | c0001 | t0017 | g0001 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01517 | hp2 | a0001 | c0001 | t0019 | g0032 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0075 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0077 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02074 | hp2 | a0001 | c0001 | t0028 | g0230 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02145 | hp2 | a0001 | c0001 | t0024 | g0121 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CDX | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0078 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0124 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0096 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0128 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0043 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02683 | hp1 | a0001 | c0001 | t0027 | g0046 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02698 | hp2 | a0001 | c0001 | t0020 | g0225 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0186 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0057 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0241 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0224 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0095 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02895 | hp2 | a0001 | c0001 | t0025 | g0131 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0223 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0120 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0076 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0043 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0233 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0063 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03239 | hp1 | a0001 | c0001 | t0018 | g0149 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0125 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0079 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03688 | hp2 | a0001 | c0001 | t0010 | g0057 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0239 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0141 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0242 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0123 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04115 | hp1 | a0001 | c0001 | t0026 | g0033 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0238 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0065 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0004 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0235 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0240 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18952 | hp2 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18961 | hp2 | a0001 | c0001 | t0011 | g0188 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18966 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18975 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18979 | hp1 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0229 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19005 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0227 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19059 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19064 | hp2 | a0001 | c0001 | t0011 | g0175 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19070 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0067 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19089 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ASW | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0061 | AFR | ASW | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0026 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20805 | hp1 | a0001 | c0001 | t0010 | g0234 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0129 | SAS | GIH | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | GIH | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0191 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0165 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| NA21309 | hp2 | a0001 | c0001 | t0023 | g0101 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0074 | REF | REF | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:49424044 | A | C | 4 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0020 others(1): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-254A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | 254 | chr15 | 49424044 | ||||||
| chr15:49424080 | T | C | 1 | a0001c0001t0021 | 1 | HG01257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | 218 | chr15 | 49424080 | ||||||
| chr15:49424281 | C | T | 1 | a0001c0001t0017 | 3 | HG01192.hp2 HG01517.hp1 HG03704.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-17C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | chr15 | 49424281 | |||||||
| chr15:49484687 | A | G | 1 | a0001c0001t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 183 | chr15 | 49484687 | ||||||
| chr15:49484760 | C | A | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(7): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 256 | chr15 | 49484760 | ||||||
| chr15:49484856 | C | T | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(3): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 352 | chr15 | 49484856 | ||||||
| chr15:49484929 | A | G | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(7): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 425 | chr15 | 49484929 | ||||||
| chr15:49485234 | T | TAC | 1 | a0001c0001t0013 | 4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*731_*732dupAC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 733 | INFO_REALIGN_3_PRIME | chr15 | 49485234 | |||||
| chr15:49485271 | A | T | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(8): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*767A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 767 | chr15 | 49485271 | ||||||
| chr15:49485473 | TA | T | 5 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0021 others(2): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*979delA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 979 | INFO_REALIGN_3_PRIME | chr15 | 49485473 | |||||
| chr15:49485703 | C | T | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0021 others(2): Show |
82 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1199C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1199 | chr15 | 49485703 | ||||||
| chr15:49485860 | C | T | 1 | a0001c0001t0015 | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1356 | chr15 | 49485860 | ||||||
| chr15:49486182 | T | C | 1 | a0001c0001t0012 | 5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1678T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1678 | chr15 | 49486182 | ||||||
| chr15:49486225 | C | T | 1 | a0001c0001t0026 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1721 | chr15 | 49486225 | ||||||
| chr15:49486424 | T | C | 1 | a0001c0001t0018 | 2 | HG00735.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1920T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1920 | chr15 | 49486424 | ||||||
| chr15:49486625 | T | A | 1 | a0001c0001t0023 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2121T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2121 | chr15 | 49486625 | ||||||
| chr15:49486937 | A | G | 1 | a0001c0001t0019 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2433A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2433 | chr15 | 49486937 | ||||||
| chr15:49487038 | T | A | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(3): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2534T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2534 | chr15 | 49487038 | ||||||
| chr15:49487079 | T | C | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(7): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2575T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2575 | chr15 | 49487079 | ||||||
| chr15:49487420 | AATT | A | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(3): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2919_*2921delTAT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2919 | INFO_REALIGN_3_PRIME | chr15 | 49487420 | |||||
| chr15:49487591 | C | T | 2 | a0001c0001t0004 a0001c0001t0018 |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3087C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3087 | chr15 | 49487591 | ||||||
| chr15:49487647 | T | G | 1 | a0001c0001t0020 | 2 | HG02698.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3143T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3143 | chr15 | 49487647 | ||||||
| chr15:49487706 | A | G | 1 | a0001c0001t0022 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3202A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3202 | chr15 | 49487706 | ||||||
| chr15:49487737 | C | T | 1 | a0001c0001t0006 | 21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3233C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3233 | chr15 | 49487737 | ||||||
| chr15:49487805 | C | A | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 |
39 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3301C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3301 | chr15 | 49487805 | ||||||
| chr15:49488162 | T | C | 1 | a0001c0001t0024 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3658T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3658 | chr15 | 49488162 | ||||||
| chr15:49488165 | G | A | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(3): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3661G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3661 | chr15 | 49488165 | ||||||
| chr15:49488183 | G | C | 1 | a0001c0001t0025 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3679G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3679 | chr15 | 49488183 | ||||||
| chr15:49488543 | T | C | 3 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0014 |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4039T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4039 | chr15 | 49488543 | ||||||
| chr15:49488598 | TATC | T | 1 | a0001c0001t0016 | 3 | HG00558.hp1 NA18952.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4097_*4099delCAT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4097 | INFO_REALIGN_3_PRIME | chr15 | 49488598 | |||||
| chr15:49488624 | A | C | 12 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(9): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4120A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4120 | chr15 | 49488624 | ||||||
| chr15:49488633 | T | C | 2 | a0001c0001t0015 a0001c0001t0020 |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4129T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4129 | chr15 | 49488633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:49423558 | A | ACTAT | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-267+119_-267+122d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 49423558 | ||||||
| chr15:49423728 | A | G | 3 | a0001c0001t0005g0220 a0001c0001t0005g0221 a0001c0001t0005g0222 |
3 | HG00733.hp2 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-267+288A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423728 | |||||||
| chr15:49423810 | A | G | 68 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(65): Show |
103 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-266-222A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423810 | |||||||
| chr15:49423820 | TG | T | 3 | a0001c0001t0004g0044 a0001c0001t0004g0169 a0001c0001t0004g0170 |
4 | HG01175.hp1 HG01358.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-266-211delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423820 | |||||||
| chr15:49423896 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-266-136G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423896 | |||||||
| chr15:49423944 | C | T | 1 | a0001c0001t0006g0020 | 3 | NA18942.hp2 NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-266-88C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423944 | |||||||
| chr15:49424648 | T | C | 148 | a0001c0001t0001g0066 a0001c0001t0001g0168 a0001c0001t0002g0002 others(145): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.286+65T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49424648 | |||||||
| chr15:49424822 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+239T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49424822 | |||||||
| chr15:49425048 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.286+465A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425048 | |||||||
| chr15:49425089 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+506G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425089 | |||||||
| chr15:49425302 | T | C | 5 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01109.hp2 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+719T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425302 | |||||||
| chr15:49425313 | A | G | 1 | a0001c0001t0004g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286+730A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425313 | |||||||
| chr15:49425395 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.286+812G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425395 | |||||||
| chr15:49425451 | G | A | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+868G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425451 | |||||||
| chr15:49425501 | C | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+918C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425501 | |||||||
| chr15:49425692 | A | G | 1 | a0001c0001t0005g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.286+1109A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425692 | |||||||
| chr15:49426009 | A | C | 1 | a0001c0001t0005g0097 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+1426A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426009 | |||||||
| chr15:49426051 | A | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+1468A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426051 | |||||||
| chr15:49426065 | GGATAATA others(3): Show |
G | 5 | a0001c0001t0008g0056 a0001c0001t0008g0226 a0001c0001t0008g0227 others(2): Show |
6 | HG00642.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+1483_286+1492d others(12): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426065 | |||||||
| chr15:49426151 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+1568C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426151 | |||||||
| chr15:49426260 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.286+1677G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426260 | |||||||
| chr15:49426322 | C | T | 23 | a0001c0001t0003g0021 a0001c0001t0003g0218 a0001c0001t0003g0219 others(20): Show |
28 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.286+1739C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426322 | |||||||
| chr15:49426381 | G | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+1798G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426381 | |||||||
| chr15:49426531 | G | T | 31 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+1948G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426531 | |||||||
| chr15:49426682 | T | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+2099T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426682 | |||||||
| chr15:49426739 | C | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+2156C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426739 | |||||||
| chr15:49426799 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+2216A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426799 | |||||||
| chr15:49427214 | A | G | 2 | a0001c0001t0014g0075 a0001c0001t0014g0096 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.286+2631A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427214 | |||||||
| chr15:49427557 | C | T | 1 | a0001c0001t0013g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286+2974C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427557 | |||||||
| chr15:49427558 | A | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+2975A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427558 | |||||||
| chr15:49427559 | T | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+2976T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427559 | |||||||
| chr15:49427597 | C | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+3014C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427597 | |||||||
| chr15:49427619 | C | A | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.286+3036C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427619 | |||||||
| chr15:49427666 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+3083G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427666 | |||||||
| chr15:49427756 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+3173A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427756 | |||||||
| chr15:49427910 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286+3327T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427910 | |||||||
| chr15:49427911 | A | T | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+3328A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427911 | |||||||
| chr15:49428051 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+3468G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428051 | |||||||
| chr15:49428224 | C | G | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+3641C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428224 | |||||||
| chr15:49428367 | T | C | 3 | a0001c0001t0010g0231 a0001c0001t0010g0232 a0001c0001t0028g0230 |
3 | HG00408.hp1 HG02074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.286+3784T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428367 | |||||||
| chr15:49428542 | T | G | 23 | a0001c0001t0002g0171 a0001c0001t0003g0010 a0001c0001t0003g0016 others(20): Show |
33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+3959T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428542 | |||||||
| chr15:49428570 | C | G | 1 | a0001c0001t0004g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+3987C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428570 | |||||||
| chr15:49428581 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+3998G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428581 | |||||||
| chr15:49428706 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.286+4123C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428706 | |||||||
| chr15:49428874 | G | A | 1 | a0001c0001t0008g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+4291G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428874 | |||||||
| chr15:49429017 | G | GTC | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+4435_286+4436i others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49429017 | ||||||
| chr15:49429207 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+4624A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429207 | |||||||
| chr15:49429477 | TC | T | 2 | a0001c0001t0005g0023 a0001c0001t0005g0098 |
3 | NA18949.hp2 NA19082.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.286+4895delC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429477 | |||||||
| chr15:49429658 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+5075G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429658 | |||||||
| chr15:49429685 | T | G | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+5102T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429685 | |||||||
| chr15:49429855 | G | T | 2 | a0001c0001t0010g0241 a0001c0001t0010g0242 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.286+5272G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429855 | |||||||
| chr15:49429872 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+5289G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429872 | |||||||
| chr15:49430267 | G | C | 1 | a0001c0001t0028g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.286+5684G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430267 | |||||||
| chr15:49430421 | G | T | 1 | a0001c0001t0003g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.286+5838G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430421 | |||||||
| chr15:49430495 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+5912G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430495 | |||||||
| chr15:49430915 | G | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+6332G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430915 | |||||||
| chr15:49431062 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.286+6479T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431062 | |||||||
| chr15:49431097 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.286+6514A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431097 | |||||||
| chr15:49431221 | G | T | 2 | a0001c0001t0015g0043 a0001c0001t0015g0165 |
3 | HG02622.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286+6638G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431221 | |||||||
| chr15:49431224 | G | A | 1 | a0001c0001t0009g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6641G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431224 | |||||||
| chr15:49431258 | G | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+6675G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431258 | |||||||
| chr15:49431424 | A | G | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+6841A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431424 | |||||||
| chr15:49431552 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+6969C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431552 | |||||||
| chr15:49431625 | A | T | 1 | a0001c0001t0014g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286+7042A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431625 | |||||||
| chr15:49431630 | T | C | 3 | a0001c0001t0013g0027 a0001c0001t0013g0076 a0001c0001t0013g0095 |
4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+7047T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431630 | |||||||
| chr15:49431684 | G | A | 23 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0030 others(20): Show |
33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+7101G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431684 | |||||||
| chr15:49431701 | C | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+7118C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431701 | |||||||
| chr15:49431980 | A | T | 1 | a0001c0001t0002g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.286+7397A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431980 | |||||||
| chr15:49431984 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0167 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286+7401C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431984 | |||||||
| chr15:49432155 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+7572T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432155 | |||||||
| chr15:49432301 | C | T | 1 | a0001c0001t0007g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286+7718C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432301 | |||||||
| chr15:49432390 | C | T | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+7807C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432390 | |||||||
| chr15:49432564 | C | G | 31 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+7981C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432564 | |||||||
| chr15:49432816 | C | A | 1 | a0001c0001t0003g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.286+8233C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432816 | |||||||
| chr15:49433008 | G | A | 1 | a0001c0001t0013g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286+8425G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433008 | |||||||
| chr15:49433018 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+8435T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433018 | |||||||
| chr15:49433025 | A | G | 2 | a0001c0001t0003g0213 a0001c0001t0003g0216 |
2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.286+8442A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433025 | |||||||
| chr15:49433069 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.286+8486T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433069 | |||||||
| chr15:49433197 | T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.286+8614T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433197 | |||||||
| chr15:49433371 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+8788C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433371 | |||||||
| chr15:49433639 | T | A | 4 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(1): Show |
6 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+9056T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433639 | |||||||
| chr15:49433643 | G | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+9060G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433643 | |||||||
| chr15:49433685 | T | C | 1 | a0001c0001t0007g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.286+9102T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433685 | |||||||
| chr15:49434085 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+9502A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434085 | |||||||
| chr15:49434135 | C | T | 1 | a0001c0001t0002g0055 | 2 | NA18962.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.286+9552C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434135 | |||||||
| chr15:49434170 | G | A | 1 | a0001c0001t0006g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.286+9587G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434170 | |||||||
| chr15:49434235 | G | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.286+9652G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434235 | |||||||
| chr15:49434286 | C | CT | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+9713dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49434286 | ||||||
| chr15:49434670 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+10087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434670 | |||||||
| chr15:49434723 | T | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10140T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434723 | |||||||
| chr15:49434777 | T | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(15): Show |
32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.286+10194T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434777 | |||||||
| chr15:49434820 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286+10237G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434820 | |||||||
| chr15:49434852 | ATAAT | A | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+10278_286+1028 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49434852 | ||||||
| chr15:49434879 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286+10296A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434879 | |||||||
| chr15:49435031 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10448A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435031 | |||||||
| chr15:49435074 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(240): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.286+10491A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435074 | |||||||
| chr15:49435243 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10660G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435243 | |||||||
| chr15:49435290 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+10707G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435290 | |||||||
| chr15:49435358 | TTAAGA | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10781_286+1078 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49435358 | ||||||
| chr15:49435432 | G | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+10849G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435432 | |||||||
| chr15:49435724 | G | T | 1 | a0001c0001t0005g0097 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+11141G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435724 | |||||||
| chr15:49435809 | C | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+11226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435809 | |||||||
| chr15:49436305 | A | G | 1 | a0001c0001t0002g0054 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.286+11722A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436305 | |||||||
| chr15:49436354 | A | G | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+11771A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436354 | |||||||
| chr15:49436562 | G | A | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+11979G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436562 | |||||||
| chr15:49436592 | A | G | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+12009A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436592 | |||||||
| chr15:49436634 | G | T | 23 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(20): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12051G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436634 | |||||||
| chr15:49436680 | A | AT | 23 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(20): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12099dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49436680 | ||||||
| chr15:49436684 | A | C | 23 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(20): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12101A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436684 | |||||||
| chr15:49436685 | G | T | 23 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(20): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12102G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436685 | |||||||
| chr15:49436689 | C | A | 23 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(20): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12106C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436689 | |||||||
| chr15:49436731 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+12148G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436731 | |||||||
| chr15:49436738 | C | T | 1 | a0001c0001t0005g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+12155C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436738 | |||||||
| chr15:49436994 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+12411G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436994 | |||||||
| chr15:49437099 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+12516T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437099 | |||||||
| chr15:49437168 | T | C | 1 | a0001c0001t0003g0030 | 2 | NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.286+12585T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437168 | |||||||
| chr15:49437728 | G | A | 83 | a0001c0001t0001g0066 a0001c0001t0002g0002 a0001c0001t0002g0005 others(80): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+13145G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437728 | |||||||
| chr15:49437809 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.286+13226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437809 | |||||||
| chr15:49437890 | A | T | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+13307A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437890 | |||||||
| chr15:49437901 | C | G | 1 | a0001c0001t0007g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.286+13318C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437901 | |||||||
| chr15:49437934 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+13351A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437934 | |||||||
| chr15:49437959 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(201): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.286+13376A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437959 | |||||||
| chr15:49437960 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(201): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.286+13377G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437960 | |||||||
| chr15:49437998 | G | A | 1 | a0001c0001t0009g0061 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286+13415G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437998 | |||||||
| chr15:49438008 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+13425G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438008 | |||||||
| chr15:49438108 | A | G | 1 | a0001c0001t0004g0029 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.286+13525A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438108 | |||||||
| chr15:49438299 | T | G | 2 | a0001c0001t0002g0012 a0001c0001t0011g0175 |
5 | HG02015.hp1 NA18980.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+13716T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438299 | |||||||
| chr15:49438346 | C | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+13763C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438346 | |||||||
| chr15:49438399 | C | G | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.286+13816C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438399 | |||||||
| chr15:49438453 | T | A | 1 | a0001c0001t0007g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286+13870T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438453 | |||||||
| chr15:49438469 | G | T | 1 | a0001c0001t0005g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.286+13886G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438469 | |||||||
| chr15:49438557 | AAT | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+13976_286+1397 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49438557 | ||||||
| chr15:49438587 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+14004T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438587 | |||||||
| chr15:49438710 | G | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+14127G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438710 | |||||||
| chr15:49438717 | C | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(201): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.286+14134C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438717 | |||||||
| chr15:49438820 | T | C | 1 | a0001c0001t0014g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286+14237T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438820 | |||||||
| chr15:49438834 | T | TGAGA | 147 | a0001c0001t0001g0066 a0001c0001t0001g0168 a0001c0001t0002g0002 others(144): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.286+14259_286+1426 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49438834 | ||||||
| chr15:49438971 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+14388C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438971 | |||||||
| chr15:49439101 | G | C | 1 | a0001c0001t0002g0177 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.286+14518G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439101 | |||||||
| chr15:49439137 | A | G | 1 | a0001c0001t0007g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286+14554A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439137 | |||||||
| chr15:49439158 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+14575T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439158 | |||||||
| chr15:49439168 | G | A | 1 | a0001c0001t0018g0080 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.286+14585G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439168 | |||||||
| chr15:49439177 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+14594C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439177 | |||||||
| chr15:49439271 | G | C | 2 | a0001c0001t0003g0031 a0001c0001t0003g0107 |
3 | NA18612.hp1 NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.286+14688G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439271 | |||||||
| chr15:49439419 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+14836T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439419 | |||||||
| chr15:49439453 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.286+14870T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439453 | |||||||
| chr15:49439727 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15144G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439727 | |||||||
| chr15:49440210 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15627T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440210 | |||||||
| chr15:49440217 | T | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+15634T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440217 | |||||||
| chr15:49440383 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15800T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440383 | |||||||
| chr15:49440512 | T | A | 5 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(2): Show |
7 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+15929T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440512 | |||||||
| chr15:49440679 | C | G | 1 | a0001c0001t0005g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.286+16096C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440679 | |||||||
| chr15:49440845 | A | G | 1 | a0001c0001t0021g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.286+16262A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440845 | |||||||
| chr15:49440861 | T | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(6): Show |
12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+16278T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440861 | |||||||
| chr15:49440876 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+16293T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440876 | |||||||
| chr15:49440916 | G | A | 1 | a0001c0001t0005g0097 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+16333G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440916 | |||||||
| chr15:49440961 | A | T | 1 | a0001c0001t0002g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+16378A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440961 | |||||||
| chr15:49441549 | C | T | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+16966C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49441549 | |||||||
| chr15:49441808 | C | T | 1 | a0001c0001t0012g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286+17225C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49441808 | |||||||
| chr15:49442067 | T | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(15): Show |
32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.286+17484T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442067 | |||||||
| chr15:49442122 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286+17539A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442122 | |||||||
| chr15:49442127 | T | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.286+17544T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442127 | |||||||
| chr15:49442301 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.286+17718G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442301 | |||||||
| chr15:49442346 | C | T | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+17763C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442346 | |||||||
| chr15:49442437 | C | T | 137 | a0001c0001t0001g0066 a0001c0001t0001g0168 a0001c0001t0002g0002 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.286+17854C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442437 | |||||||
| chr15:49442494 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+17911G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442494 | |||||||
| chr15:49442516 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+17933T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442516 | |||||||
| chr15:49442538 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+17955T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442538 | |||||||
| chr15:49442543 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.286+17960C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442543 | |||||||
| chr15:49442646 | A | G | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+18063A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442646 | |||||||
| chr15:49442771 | C | T | 16 | a0001c0001t0001g0066 a0001c0001t0005g0003 a0001c0001t0005g0023 others(13): Show |
24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+18188C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442771 | |||||||
| chr15:49442915 | C | T | 171 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0168 others(168): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.286+18332C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442915 | |||||||
| chr15:49443025 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.286+18442T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443025 | |||||||
| chr15:49443100 | T | C | 55 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(52): Show |
69 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.286+18517T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443100 | |||||||
| chr15:49443171 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.286+18588T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443171 | |||||||
| chr15:49443267 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+18684C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443267 | |||||||
| chr15:49443282 | A | G | 1 | a0001c0001t0007g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286+18699A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443282 | |||||||
| chr15:49443409 | C | T | 1 | a0001c0001t0003g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.286+18826C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443409 | |||||||
| chr15:49443468 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
51 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.286+18885C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443468 | |||||||
| chr15:49443482 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+18899T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443482 | |||||||
| chr15:49443532 | C | CT | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+18951dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49443532 | ||||||
| chr15:49443542 | A | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+18959A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443542 | |||||||
| chr15:49443568 | T | C | 2 | a0001c0001t0005g0220 a0001c0001t0005g0221 |
2 | HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.286+18985T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443568 | |||||||
| chr15:49443806 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.286+19223C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443806 | |||||||
| chr15:49443924 | TC | T | 83 | a0001c0001t0001g0066 a0001c0001t0002g0002 a0001c0001t0002g0005 others(80): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+19342delC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443924 | |||||||
| chr15:49443992 | G | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0171 a0001c0001t0002g0179 others(5): Show |
14 | HG00408.hp2 HG01257.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+19409G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443992 | |||||||
| chr15:49444142 | T | G | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+19559T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444142 | |||||||
| chr15:49444222 | T | G | 2 | a0001c0001t0002g0179 a0001c0001t0021g0210 |
2 | HG01257.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.286+19639T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444222 | |||||||
| chr15:49444228 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0014g0075 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.286+19645C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444228 | |||||||
| chr15:49444367 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286+19784G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444367 | |||||||
| chr15:49444399 | T | C | 1 | a0001c0001t0009g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286+19816T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444399 | |||||||
| chr15:49444448 | T | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+19865T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444448 | |||||||
| chr15:49444554 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.286+19971T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444554 | |||||||
| chr15:49444621 | G | A | 31 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+20038G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444621 | |||||||
| chr15:49444709 | G | T | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+20126G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444709 | |||||||
| chr15:49445068 | A | G | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+20485A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445068 | |||||||
| chr15:49445309 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+20726G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445309 | |||||||
| chr15:49445337 | G | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+20754G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445337 | |||||||
| chr15:49445499 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(201): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.286+20916A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445499 | |||||||
| chr15:49445735 | T | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21152T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445735 | |||||||
| chr15:49445860 | G | A | 1 | a0001c0001t0005g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.286+21277G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445860 | |||||||
| chr15:49445961 | T | C | 5 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(2): Show |
7 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+21378T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445961 | |||||||
| chr15:49446036 | T | C | 32 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(29): Show |
43 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.286+21453T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446036 | |||||||
| chr15:49446099 | T | A | 16 | a0001c0001t0001g0066 a0001c0001t0005g0003 a0001c0001t0005g0023 others(13): Show |
24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+21516T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446099 | |||||||
| chr15:49446117 | T | C | 10 | a0001c0001t0010g0057 a0001c0001t0010g0231 a0001c0001t0010g0232 others(7): Show |
11 | HG00408.hp1 HG01255.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+21534T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446117 | |||||||
| chr15:49446137 | G | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21554G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446137 | |||||||
| chr15:49446164 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21581A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446164 | |||||||
| chr15:49446173 | C | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+21590C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446173 | |||||||
| chr15:49446196 | T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.286+21613T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446196 | |||||||
| chr15:49446270 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.286+21687T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446270 | |||||||
| chr15:49446331 | C | T | 1 | a0001c0001t0014g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286+21748C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446331 | |||||||
| chr15:49446345 | C | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+21762C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446345 | |||||||
| chr15:49446492 | G | C | 1 | a0001c0001t0008g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+21909G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446492 | |||||||
| chr15:49446585 | AG | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22005delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49446585 | ||||||
| chr15:49446792 | A | C | 1 | a0001c0001t0001g0042 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286+22209A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446792 | |||||||
| chr15:49446850 | T | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+22267T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446850 | |||||||
| chr15:49446926 | C | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22343C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446926 | |||||||
| chr15:49446928 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22345G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446928 | |||||||
| chr15:49447147 | A | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+22564A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447147 | |||||||
| chr15:49447153 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(224): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.286+22570T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447153 | |||||||
| chr15:49447271 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+22688A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447271 | |||||||
| chr15:49447365 | G | C | 1 | a0001c0001t0003g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.286+22782G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447365 | |||||||
| chr15:49447511 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22928T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447511 | |||||||
| chr15:49447521 | T | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+22938T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447521 | |||||||
| chr15:49447763 | C | T | 1 | a0001c0001t0014g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286+23180C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447763 | |||||||
| chr15:49447769 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+23186C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447769 | |||||||
| chr15:49448035 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+23452C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448035 | |||||||
| chr15:49448107 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+23524A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448107 | |||||||
| chr15:49448420 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+23837T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448420 | |||||||
| chr15:49448674 | C | CAT | 11 | a0001c0001t0008g0223 a0001c0001t0012g0015 a0001c0001t0012g0077 others(8): Show |
14 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+24105_286+2410 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49448674 | ||||||
| chr15:49448761 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+24178G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448761 | |||||||
| chr15:49448866 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+24283G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448866 | |||||||
| chr15:49448874 | T | C | 32 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(29): Show |
43 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.286+24291T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448874 | |||||||
| chr15:49448918 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+24335A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448918 | |||||||
| chr15:49449102 | TCAAA | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+24522_286+2452 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49449102 | ||||||
| chr15:49449188 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+24605T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449188 | |||||||
| chr15:49449557 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.286+24974G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449557 | |||||||
| chr15:49449580 | T | A | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+24997T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449580 | |||||||
| chr15:49449651 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+25068G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449651 | |||||||
| chr15:49449806 | T | TATAA | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(227): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.286+25225_286+2522 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49449806 | ||||||
| chr15:49450046 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.286+25463T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450046 | |||||||
| chr15:49450297 | A | C | 146 | a0001c0001t0001g0066 a0001c0001t0001g0168 a0001c0001t0002g0002 others(143): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.286+25714A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450297 | |||||||
| chr15:49450483 | A | G | 1 | a0001c0001t0009g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.286+25900A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450483 | |||||||
| chr15:49450636 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+26053G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450636 | |||||||
| chr15:49450714 | A | G | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+26131A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450714 | |||||||
| chr15:49450748 | AT | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+26166delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450748 | |||||||
| chr15:49450758 | G | A | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+26175G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450758 | |||||||
| chr15:49450872 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+26289A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450872 | |||||||
| chr15:49450881 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+26298C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450881 | |||||||
| chr15:49451153 | A | C | 2 | a0001c0001t0002g0093 a0001c0001t0004g0028 |
3 | HG01099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.286+26570A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451153 | |||||||
| chr15:49451198 | C | T | 23 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0030 others(20): Show |
33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+26615C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451198 | |||||||
| chr15:49451379 | G | T | 1 | a0001c0001t0006g0132 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.286+26796G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451379 | |||||||
| chr15:49451385 | T | C | 83 | a0001c0001t0001g0066 a0001c0001t0002g0002 a0001c0001t0002g0005 others(80): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+26802T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451385 | |||||||
| chr15:49451431 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+26848C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451431 | |||||||
| chr15:49451814 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+27231C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451814 | |||||||
| chr15:49451891 | G | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+27308G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451891 | |||||||
| chr15:49452179 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+27596C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452179 | |||||||
| chr15:49452186 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+27603T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452186 | |||||||
| chr15:49452252 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+27669T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452252 | |||||||
| chr15:49452273 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.286+27690G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452273 | |||||||
| chr15:49452370 | T | C | 149 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0168 others(146): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.286+27787T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452370 | |||||||
| chr15:49452522 | T | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+27939T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452522 | |||||||
| chr15:49452636 | C | A | 3 | a0001c0001t0010g0231 a0001c0001t0010g0232 a0001c0001t0028g0230 |
3 | HG00408.hp1 HG02074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.286+28053C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452636 | |||||||
| chr15:49452662 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+28079T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452662 | |||||||
| chr15:49452699 | G | A | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+28116G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452699 | |||||||
| chr15:49452744 | C | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(6): Show |
12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+28161C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452744 | |||||||
| chr15:49453117 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+28534A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453117 | |||||||
| chr15:49453223 | G | A | 31 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+28640G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453223 | |||||||
| chr15:49453235 | C | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01109.hp2 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+28652C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453235 | |||||||
| chr15:49453378 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+28795A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453378 | |||||||
| chr15:49453480 | C | G | 21 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0030 others(18): Show |
30 | HG01943.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.286+28897C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453480 | |||||||
| chr15:49453514 | T | G | 1 | a0001c0001t0003g0030 | 2 | NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.286+28931T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453514 | |||||||
| chr15:49453556 | C | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+28973C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453556 | |||||||
| chr15:49453623 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.286+29040T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453623 | |||||||
| chr15:49453642 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+29059C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453642 | |||||||
| chr15:49453684 | C | T | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+29101C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453684 | |||||||
| chr15:49453813 | A | G | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+29230A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453813 | |||||||
| chr15:49453908 | G | A | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.287-29243G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453908 | |||||||
| chr15:49453922 | C | A | 1 | a0001c0001t0005g0220 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.287-29229C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453922 | |||||||
| chr15:49453971 | A | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-29180A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453971 | |||||||
| chr15:49454167 | T | A | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-28984T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454167 | |||||||
| chr15:49454274 | C | A | 1 | a0001c0001t0023g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-28877C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454274 | |||||||
| chr15:49454319 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.287-28832C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454319 | |||||||
| chr15:49454377 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-28774T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454377 | |||||||
| chr15:49454898 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-28253T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454898 | |||||||
| chr15:49455029 | G | A | 1 | a0001c0001t0010g0233 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-28122G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455029 | |||||||
| chr15:49455039 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-28112G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455039 | |||||||
| chr15:49455090 | CAT | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-28058_287-2805 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49455090 | ||||||
| chr15:49455139 | T | C | 1 | a0001c0001t0004g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.287-28012T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455139 | |||||||
| chr15:49455148 | G | A | 31 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.287-28003G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455148 | |||||||
| chr15:49455288 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.287-27863G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455288 | |||||||
| chr15:49455426 | C | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(15): Show |
32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.287-27725C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455426 | |||||||
| chr15:49455466 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-27685C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455466 | |||||||
| chr15:49455537 | T | C | 1 | a0001c0001t0003g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.287-27614T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455537 | |||||||
| chr15:49455556 | G | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(15): Show |
32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.287-27595G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455556 | |||||||
| chr15:49455606 | C | T | 1 | a0001c0001t0025g0131 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.287-27545C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455606 | |||||||
| chr15:49455632 | TTAATC | T | 9 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0068 others(6): Show |
15 | HG00558.hp1 HG01243.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-27514_287-2751 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49455632 | ||||||
| chr15:49455773 | T | C | 23 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(20): Show |
26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-27378T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455773 | |||||||
| chr15:49455926 | A | G | 16 | a0001c0001t0001g0066 a0001c0001t0005g0003 a0001c0001t0005g0023 others(13): Show |
24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-27225A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455926 | |||||||
| chr15:49456065 | A | T | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-27086A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456065 | |||||||
| chr15:49456081 | G | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-27070G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456081 | |||||||
| chr15:49456123 | A | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0226 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-27028A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456123 | |||||||
| chr15:49456168 | C | G | 66 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(63): Show |
101 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.287-26983C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456168 | |||||||
| chr15:49456328 | G | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(6): Show |
12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-26823G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456328 | |||||||
| chr15:49456416 | G | A | 54 | a0001c0001t0001g0168 a0001c0001t0002g0091 a0001c0001t0002g0093 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-26735G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456416 | |||||||
| chr15:49456593 | C | G | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.287-26558C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456593 | |||||||
| chr15:49456658 | A | C | 1 | a0001c0001t0002g0209 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.287-26493A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456658 | |||||||
| chr15:49456761 | T | C | 3 | a0001c0001t0008g0223 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-26390T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456761 | |||||||
| chr15:49456899 | C | T | 1 | a0001c0001t0028g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.287-26252C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456899 | |||||||
| chr15:49457052 | A | G | 1 | a0001c0001t0008g0240 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.287-26099A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457052 | |||||||
| chr15:49457107 | G | T | 28 | a0001c0001t0002g0091 a0001c0001t0002g0093 a0001c0001t0002g0208 others(25): Show |
36 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.287-26044G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457107 | |||||||
| chr15:49457243 | C | T | 1 | a0001c0001t0004g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.287-25908C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457243 | |||||||
| chr15:49457278 | C | T | 17 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(14): Show |
19 | HG00408.hp1 HG01109.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-25873C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457278 | |||||||
| chr15:49457351 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(78): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.287-25800T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457351 | |||||||
| chr15:49457529 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(86): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-25622A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457529 | |||||||
| chr15:49457538 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(64): Show |
99 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.287-25613C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457538 | |||||||
| chr15:49457581 | T | A | 1 | a0001c0001t0016g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.287-25570T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457581 | |||||||
| chr15:49457621 | T | C | 1 | a0001c0001t0008g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287-25530T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457621 | |||||||
| chr15:49457877 | CT | C | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-25273delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457877 | |||||||
| chr15:49457882 | C | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0209 a0001c0001t0002g0217 |
3 | HG00609.hp2 NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.287-25269C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457882 | |||||||
| chr15:49457959 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-25192T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457959 | |||||||
| chr15:49458210 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(168): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-24941A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458210 | |||||||
| chr15:49458231 | T | C | 76 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.287-24920T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458231 | |||||||
| chr15:49458283 | A | AC | 19 | a0001c0001t0002g0193 a0001c0001t0005g0003 a0001c0001t0005g0023 others(16): Show |
27 | HG00558.hp1 HG00733.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-24861dupC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49458283 | ||||||
| chr15:49458389 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.287-24762C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458389 | |||||||
| chr15:49458987 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-24164C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458987 | |||||||
| chr15:49458988 | G | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-24163G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458988 | |||||||
| chr15:49459028 | C | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-24123C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459028 | |||||||
| chr15:49459221 | A | G | 3 | a0001c0001t0007g0039 a0001c0001t0007g0129 a0001c0001t0007g0163 |
4 | HG02451.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-23930A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459221 | |||||||
| chr15:49459361 | A | G | 1 | a0001c0001t0007g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.287-23790A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459361 | |||||||
| chr15:49459429 | T | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-23722T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459429 | |||||||
| chr15:49459476 | GAA | G | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-23672_287-2367 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49459476 | ||||||
| chr15:49459511 | A | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-23640A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459511 | |||||||
| chr15:49459542 | CT | C | 11 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(8): Show |
13 | HG00558.hp2 HG00642.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-23608delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459542 | |||||||
| chr15:49459656 | A | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-23495A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459656 | |||||||
| chr15:49459695 | C | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-23456C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459695 | |||||||
| chr15:49459933 | C | A | 1 | a0001c0001t0006g0124 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.287-23218C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459933 | |||||||
| chr15:49460066 | C | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-23085C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460066 | |||||||
| chr15:49460497 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(168): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-22654T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460497 | |||||||
| chr15:49460548 | T | C | 1 | a0001c0001t0013g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.287-22603T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460548 | |||||||
| chr15:49460759 | T | C | 1 | a0001c0001t0014g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.287-22392T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460759 | |||||||
| chr15:49461079 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-22072C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461079 | |||||||
| chr15:49461335 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-21816T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461335 | |||||||
| chr15:49461450 | C | T | 3 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 |
5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-21701C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461450 | |||||||
| chr15:49461564 | C | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-21587C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461564 | |||||||
| chr15:49461656 | A | G | 1 | a0001c0001t0004g0089 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.287-21495A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461656 | |||||||
| chr15:49461951 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.287-21200C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461951 | |||||||
| chr15:49462254 | G | A | 23 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(20): Show |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-20897G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462254 | |||||||
| chr15:49462365 | A | G | 86 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(83): Show |
125 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.287-20786A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462365 | |||||||
| chr15:49462436 | G | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-20715G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462436 | |||||||
| chr15:49462527 | T | C | 1 | a0001c0001t0010g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.287-20624T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462527 | |||||||
| chr15:49462547 | C | G | 83 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(80): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.287-20604C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462547 | |||||||
| chr15:49462599 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-20552T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462599 | |||||||
| chr15:49462692 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.287-20459C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462692 | |||||||
| chr15:49462822 | G | A | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-20329G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462822 | |||||||
| chr15:49462870 | TAA | T | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-20279_287-2027 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49462870 | ||||||
| chr15:49462955 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.287-20196G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462955 | |||||||
| chr15:49463099 | A | G | 10 | a0001c0001t0001g0168 a0001c0001t0010g0057 a0001c0001t0010g0231 others(7): Show |
11 | HG00408.hp1 HG01255.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-20052A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463099 | |||||||
| chr15:49463208 | C | T | 1 | a0001c0001t0003g0034 | 2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.287-19943C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463208 | |||||||
| chr15:49463245 | T | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19906T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463245 | |||||||
| chr15:49463252 | C | A | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-19899C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463252 | |||||||
| chr15:49463371 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-19780T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463371 | |||||||
| chr15:49463432 | T | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-19719T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463432 | |||||||
| chr15:49463476 | G | A | 5 | a0001c0001t0004g0044 a0001c0001t0004g0082 a0001c0001t0004g0083 others(2): Show |
6 | HG00741.hp1 HG01175.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-19675G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463476 | |||||||
| chr15:49463550 | C | CA | 31 | a0001c0001t0004g0026 a0001c0001t0004g0084 a0001c0001t0005g0003 others(28): Show |
44 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.287-19585dupA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | ||||||
| chr15:49463550 | C | CAAA | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.287-19587_287-1958 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | ||||||
| chr15:49463550 | C | CAAAA | 18 | a0001c0001t0002g0189 a0001c0001t0002g0197 a0001c0001t0002g0206 others(15): Show |
25 | HG01169.hp1 HG01255.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.287-19588_287-1958 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | ||||||
| chr15:49463550 | C | CAAAAA | 6 | a0001c0001t0007g0196 a0001c0001t0012g0077 a0001c0001t0013g0027 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-19589_287-1958 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | ||||||
| chr15:49463567 | T | A | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-19584T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463567 | |||||||
| chr15:49463645 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19506G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463645 | |||||||
| chr15:49463884 | A | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19267A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463884 | |||||||
| chr15:49463932 | T | A | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-19219T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463932 | |||||||
| chr15:49463932 | T | TTTTG | 74 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(71): Show |
110 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.287-19210_287-1920 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463932 | ||||||
| chr15:49464064 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-19087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464064 | |||||||
| chr15:49464178 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-18973T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464178 | |||||||
| chr15:49464283 | G | T | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-18868G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464283 | |||||||
| chr15:49464572 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(60): Show |
96 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.287-18579T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464572 | |||||||
| chr15:49464789 | C | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-18362C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464789 | |||||||
| chr15:49464812 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0208 a0001c0001t0002g0215 |
4 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-18339C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464812 | |||||||
| chr15:49464843 | A | G | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-18308A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464843 | |||||||
| chr15:49464900 | T | C | 1 | a0001c0001t0007g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-18251T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464900 | |||||||
| chr15:49464911 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-18240C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464911 | |||||||
| chr15:49465026 | A | G | 3 | a0001c0001t0013g0027 a0001c0001t0013g0076 a0001c0001t0013g0095 |
4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-18125A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465026 | |||||||
| chr15:49465188 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(170): Show |
253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.287-17963A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465188 | |||||||
| chr15:49465269 | A | G | 47 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(44): Show |
66 | HG00558.hp1 HG00733.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.287-17882A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465269 | |||||||
| chr15:49465304 | C | CT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(85): Show |
128 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-17833dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49465304 | ||||||
| chr15:49465561 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-17590T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465561 | |||||||
| chr15:49465591 | AAAAG | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(78): Show |
120 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.287-17558_287-1755 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49465591 | ||||||
| chr15:49465592 | A | AGAGACCT others(4994): Show |
1 | a0001c0001t0002g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-17559_287-1755 others(5005): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465592 | |||||||
| chr15:49465595 | G | A | 1 | a0001c0001t0002g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-17556G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465595 | |||||||
| chr15:49465785 | T | A | 64 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.287-17366T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465785 | |||||||
| chr15:49465801 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0211 a0001c0001t0027g0046 |
3 | HG02683.hp1 HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.287-17350C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465801 | |||||||
| chr15:49465829 | T | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-17322T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465829 | |||||||
| chr15:49465974 | A | G | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-17177A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465974 | |||||||
| chr15:49466231 | G | A | 2 | a0001c0001t0004g0085 a0001c0001t0004g0092 |
2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.287-16920G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466231 | |||||||
| chr15:49466302 | T | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-16849T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466302 | |||||||
| chr15:49466496 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.287-16655T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466496 | |||||||
| chr15:49466532 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-16619T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466532 | |||||||
| chr15:49466539 | T | C | 1 | a0001c0001t0020g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.287-16612T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466539 | |||||||
| chr15:49466794 | T | C | 4 | a0001c0001t0003g0010 a0001c0001t0003g0112 a0001c0001t0003g0113 others(1): Show |
7 | NA18961.hp1 NA18973.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-16357T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466794 | |||||||
| chr15:49467083 | G | T | 1 | a0001c0001t0004g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.287-16068G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467083 | |||||||
| chr15:49467187 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.287-15964G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467187 | |||||||
| chr15:49467331 | G | A | 1 | a0001c0001t0019g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-15820G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467331 | |||||||
| chr15:49467460 | C | CT | 2 | a0001c0001t0007g0039 a0001c0001t0007g0163 |
3 | HG02451.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-15690dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49467460 | ||||||
| chr15:49467688 | T | C | 3 | a0001c0001t0007g0214 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.287-15463T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467688 | |||||||
| chr15:49467732 | A | G | 2 | a0001c0001t0009g0022 a0001c0001t0009g0063 |
3 | HG01884.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-15419A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467732 | |||||||
| chr15:49468144 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-15007A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468144 | |||||||
| chr15:49468149 | T | C | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-15002T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468149 | |||||||
| chr15:49468228 | G | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-14923G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468228 | |||||||
| chr15:49468349 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(168): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-14802A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468349 | |||||||
| chr15:49468692 | A | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-14459A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468692 | |||||||
| chr15:49468807 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-14344C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468807 | |||||||
| chr15:49468836 | G | A | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-14315G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468836 | |||||||
| chr15:49468867 | A | T | 11 | a0001c0001t0006g0004 a0001c0001t0006g0020 a0001c0001t0006g0035 others(8): Show |
21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-14284A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468867 | |||||||
| chr15:49469191 | A | G | 1 | a0001c0001t0019g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-13960A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469191 | |||||||
| chr15:49469564 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0003g0109 |
2 | NA18966.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.287-13587T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469564 | |||||||
| chr15:49469648 | C | A | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-13503C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469648 | |||||||
| chr15:49469791 | A | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-13360A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469791 | |||||||
| chr15:49469965 | T | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0175 a0001c0001t0011g0188 |
6 | NA18957.hp1 NA18961.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13186T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469965 | |||||||
| chr15:49470141 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-13010A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470141 | |||||||
| chr15:49470245 | T | TAACACTG others(2): Show |
218 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(215): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.287-12898_287-1289 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49470245 | ||||||
| chr15:49470417 | T | C | 1 | a0001c0001t0006g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.287-12734T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470417 | |||||||
| chr15:49470497 | A | G | 1 | a0001c0001t0004g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.287-12654A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470497 | |||||||
| chr15:49470570 | C | T | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-12581C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470570 | |||||||
| chr15:49470736 | G | A | 11 | a0001c0001t0004g0169 a0001c0001t0012g0015 a0001c0001t0012g0077 others(8): Show |
14 | HG01255.hp1 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-12415G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470736 | |||||||
| chr15:49470916 | G | A | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-12235G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470916 | |||||||
| chr15:49470925 | C | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-12226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470925 | |||||||
| chr15:49470958 | T | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-12193T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470958 | |||||||
| chr15:49471114 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-12037T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471114 | |||||||
| chr15:49471269 | T | TG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(196): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.287-11882_287-1188 others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471269 | |||||||
| chr15:49471283 | G | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-11868G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471283 | |||||||
| chr15:49471309 | A | G | 1 | a0001c0001t0005g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.287-11842A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471309 | |||||||
| chr15:49471386 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-11765A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471386 | |||||||
| chr15:49471484 | A | AAAT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0100 a0001c0001t0001g0102 others(63): Show |
86 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.287-11620_287-1161 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | A | AAATAAT | 16 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(13): Show |
16 | HG01099.hp1 HG01884.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-11623_287-1161 others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | A | AAATAATA others(2): Show |
13 | a0001c0001t0001g0164 a0001c0001t0002g0002 a0001c0001t0002g0051 others(10): Show |
13 | HG01081.hp2 HG01891.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-11626_287-1161 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | AAAT | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
46 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-11620_287-1161 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | AAATAAT | A | 12 | a0001c0001t0003g0031 a0001c0001t0003g0107 a0001c0001t0003g0219 others(9): Show |
16 | HG00733.hp2 HG02273.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-11623_287-1161 others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | AAATAATA others(2): Show |
A | 44 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(41): Show |
58 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.287-11626_287-1161 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | AAATAATA others(5): Show |
A | 18 | a0001c0001t0001g0138 a0001c0001t0004g0008 a0001c0001t0004g0028 others(15): Show |
25 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-11629_287-1161 others(16): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471484 | AAATAATA others(8): Show |
A | 3 | a0001c0001t0001g0135 a0001c0001t0020g0224 a0001c0001t0020g0225 |
3 | HG01358.hp1 HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11632_287-1161 others(19): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | ||||||
| chr15:49471520 | T | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11631T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471520 | |||||||
| chr15:49471537 | C | A | 1 | a0001c0001t0002g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.287-11614C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471537 | |||||||
| chr15:49471546 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287-11605T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471546 | |||||||
| chr15:49471660 | C | A | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11491C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471660 | |||||||
| chr15:49471722 | C | G | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11429C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471722 | |||||||
| chr15:49471768 | C | T | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-11383C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471768 | |||||||
| chr15:49471885 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287-11266A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471885 | |||||||
| chr15:49471904 | G | A | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-11247G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471904 | |||||||
| chr15:49471935 | A | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-11216A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471935 | |||||||
| chr15:49471965 | A | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11186A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471965 | |||||||
| chr15:49472020 | GA | G | 212 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(209): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.287-11117delA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472020 | ||||||
| chr15:49472020 | GAA | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-11118_287-1111 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472020 | ||||||
| chr15:49472110 | T | C | 1 | a0001c0001t0005g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-11041T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472110 | |||||||
| chr15:49472225 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-10926T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472225 | |||||||
| chr15:49472442 | A | G | 11 | a0001c0001t0006g0004 a0001c0001t0006g0020 a0001c0001t0006g0035 others(8): Show |
21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-10709A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472442 | |||||||
| chr15:49472754 | A | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-10397A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472754 | |||||||
| chr15:49472804 | A | T | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-10347A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472804 | |||||||
| chr15:49472845 | C | G | 2 | a0001c0001t0001g0119 a0001c0001t0019g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-10306C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472845 | |||||||
| chr15:49472909 | GTACCA | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-10238_287-1023 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472909 | ||||||
| chr15:49473072 | A | G | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-10079A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473072 | |||||||
| chr15:49473131 | A | C | 1 | a0001c0001t0002g0192 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.287-10020A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473131 | |||||||
| chr15:49473171 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-9980C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473171 | |||||||
| chr15:49473182 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0163 |
3 | HG02451.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-9969G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473182 | |||||||
| chr15:49473229 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-9922C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473229 | |||||||
| chr15:49473255 | CATG | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-9889_287-9887d others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49473255 | ||||||
| chr15:49473370 | T | A | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9781T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473370 | |||||||
| chr15:49473427 | T | C | 1 | a0001c0001t0004g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.287-9724T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473427 | |||||||
| chr15:49473543 | T | C | 2 | a0001c0001t0010g0231 a0001c0001t0010g0232 |
2 | HG00408.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.287-9608T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473543 | |||||||
| chr15:49473565 | C | T | 64 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.287-9586C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473565 | |||||||
| chr15:49473581 | G | A | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-9570G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473581 | |||||||
| chr15:49473617 | C | T | 2 | a0001c0001t0014g0075 a0001c0001t0014g0096 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.287-9534C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473617 | |||||||
| chr15:49473620 | A | G | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-9531A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473620 | |||||||
| chr15:49473706 | G | T | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-9445G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473706 | |||||||
| chr15:49474054 | C | A | 23 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(20): Show |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-9097C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474054 | |||||||
| chr15:49474152 | C | T | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8999C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474152 | |||||||
| chr15:49474286 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0126 others(2): Show |
8 | HG01243.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-8865C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474286 | |||||||
| chr15:49474588 | T | A | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-8563T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474588 | |||||||
| chr15:49474660 | G | T | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-8491G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474660 | |||||||
| chr15:49474771 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-8380G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474771 | |||||||
| chr15:49474823 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0010g0232 |
2 | HG00408.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.287-8328G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474823 | |||||||
| chr15:49474826 | C | T | 2 | a0001c0001t0003g0047 a0001c0001t0028g0230 |
3 | HG02074.hp2 HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.287-8325C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474826 | |||||||
| chr15:49474869 | C | T | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8282C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474869 | |||||||
| chr15:49474886 | C | A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(48): Show |
81 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.287-8265C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474886 | |||||||
| chr15:49474937 | C | T | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8214C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474937 | |||||||
| chr15:49474964 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.287-8187T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474964 | |||||||
| chr15:49474996 | A | AAAT | 20 | a0001c0001t0005g0003 a0001c0001t0005g0023 a0001c0001t0005g0024 others(17): Show |
28 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-8153_287-8152i others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49474996 | ||||||
| chr15:49474998 | AAGAT | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-8149_287-8146d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49474998 | ||||||
| chr15:49475004 | G | T | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-8147G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475004 | |||||||
| chr15:49475120 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-8031T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475120 | |||||||
| chr15:49475273 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-7878T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475273 | |||||||
| chr15:49475423 | G | A | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-7728G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475423 | |||||||
| chr15:49475576 | A | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-7575A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475576 | |||||||
| chr15:49475614 | A | AT | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-7531dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49475614 | ||||||
| chr15:49475689 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.287-7462C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475689 | |||||||
| chr15:49475728 | T | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-7423T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475728 | |||||||
| chr15:49475927 | C | T | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-7224C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475927 | |||||||
| chr15:49476023 | T | A | 1 | a0001c0001t0002g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.287-7128T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476023 | |||||||
| chr15:49476077 | T | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-7074T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476077 | |||||||
| chr15:49476164 | G | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6987G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476164 | |||||||
| chr15:49476171 | A | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6980A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476171 | |||||||
| chr15:49476212 | G | GTTTT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0136 a0001c0001t0001g0142 others(1): Show |
6 | HG01074.hp2 HG03017.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-6938_287-6935d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | ||||||
| chr15:49476212 | G | GTTTTT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0134 others(8): Show |
18 | HG01099.hp2 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-6935_287-6934i others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | ||||||
| chr15:49476212 | G | GTTTTTT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0130 others(6): Show |
14 | HG00323.hp2 HG01175.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-6935_287-6934i others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | ||||||
| chr15:49476217 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-6934G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476217 | |||||||
| chr15:49476219 | TTTTTTGT others(6): Show |
T | 1 | a0001c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.287-6926_287-6914d others(15): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476219 | ||||||
| chr15:49476225 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-6926G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476225 | |||||||
| chr15:49476230 | TG | T | 105 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(102): Show |
149 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.287-6919delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476230 | ||||||
| chr15:49476231 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
46 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.287-6920G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476231 | |||||||
| chr15:49476231 | GGT | G | 3 | a0001c0001t0002g0055 a0001c0001t0020g0224 a0001c0001t0020g0225 |
4 | HG02698.hp2 HG02738.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-6919_287-6918d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476231 | |||||||
| chr15:49476232 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(64): Show |
99 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.287-6919G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476232 | |||||||
| chr15:49476237 | T | G | 1 | a0001c0001t0008g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.287-6914T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476237 | |||||||
| chr15:49476346 | G | T | 1 | a0001c0001t0002g0204 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.287-6805G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476346 | |||||||
| chr15:49476462 | T | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-6689T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476462 | |||||||
| chr15:49476522 | A | C | 2 | a0001c0001t0005g0023 a0001c0001t0005g0098 |
3 | NA18949.hp2 NA19082.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.287-6629A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476522 | |||||||
| chr15:49476606 | T | TAAC | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6543_287-6542i others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476606 | ||||||
| chr15:49476624 | T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-6527T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476624 | |||||||
| chr15:49476635 | CATAA | C | 9 | a0001c0001t0008g0056 a0001c0001t0008g0058 a0001c0001t0008g0223 others(6): Show |
11 | HG00642.hp1 HG02040.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-6507_287-6504d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476635 | ||||||
| chr15:49476825 | T | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6326T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476825 | |||||||
| chr15:49476921 | G | A | 1 | a0001c0001t0007g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-6230G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476921 | |||||||
| chr15:49476937 | G | A | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6214G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476937 | |||||||
| chr15:49477008 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
53 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.287-6143G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477008 | |||||||
| chr15:49477020 | A | G | 1 | a0001c0001t0028g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.287-6131A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477020 | |||||||
| chr15:49477037 | G | C | 8 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0059 others(5): Show |
11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-6114G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477037 | |||||||
| chr15:49477060 | G | GA | 7 | a0001c0001t0001g0139 a0001c0001t0003g0111 a0001c0001t0008g0058 others(4): Show |
9 | HG02135.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-6076dupA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49477060 | ||||||
| chr15:49477060 | G | GAAA | 76 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.287-6078_287-6076d others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49477060 | ||||||
| chr15:49477169 | C | G | 1 | a0001c0001t0002g0184 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287-5982C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477169 | |||||||
| chr15:49477172 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-5979C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477172 | |||||||
| chr15:49477265 | G | C | 1 | a0001c0001t0008g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.287-5886G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477265 | |||||||
| chr15:49477371 | T | C | 58 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(55): Show |
79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-5780T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477371 | |||||||
| chr15:49477412 | A | G | 1 | a0001c0001t0010g0233 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-5739A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477412 | |||||||
| chr15:49477560 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0019g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-5591T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477560 | |||||||
| chr15:49477619 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0019g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-5532G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477619 | |||||||
| chr15:49477805 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287-5346G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477805 | |||||||
| chr15:49477911 | A | G | 1 | a0001c0001t0002g0054 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.287-5240A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477911 | |||||||
| chr15:49477972 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.287-5179T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477972 | |||||||
| chr15:49478070 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-5081A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478070 | |||||||
| chr15:49478155 | G | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-4996G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478155 | |||||||
| chr15:49478419 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-4732G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478419 | |||||||
| chr15:49478457 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-4694C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478457 | |||||||
| chr15:49478592 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287-4559A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478592 | |||||||
| chr15:49478609 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-4542C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478609 | |||||||
| chr15:49478755 | T | G | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-4396T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478755 | |||||||
| chr15:49478860 | T | C | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-4291T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478860 | |||||||
| chr15:49478965 | T | A | 1 | a0001c0001t0002g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.287-4186T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478965 | |||||||
| chr15:49479243 | T | TTC | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-3898_287-3897d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479243 | ||||||
| chr15:49479287 | T | C | 29 | a0001c0001t0005g0003 a0001c0001t0005g0023 a0001c0001t0005g0024 others(26): Show |
39 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.287-3864T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479287 | |||||||
| chr15:49479360 | G | A | 84 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(81): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-3791G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479360 | |||||||
| chr15:49479363 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(239): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.287-3788A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479363 | |||||||
| chr15:49479423 | C | G | 1 | a0001c0001t0019g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-3728C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479423 | |||||||
| chr15:49479451 | G | A | 23 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(20): Show |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-3700G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479451 | |||||||
| chr15:49479532 | T | C | 1 | a0001c0001t0005g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-3619T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479532 | |||||||
| chr15:49479598 | TG | T | 25 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(22): Show |
36 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.287-3552delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479598 | |||||||
| chr15:49479599 | G | GT | 24 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0040 others(21): Show |
34 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-3523dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | G | GTT | 6 | a0001c0001t0006g0020 a0001c0001t0006g0035 a0001c0001t0006g0123 others(3): Show |
6 | HG03139.hp2 HG03942.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-3524_287-3523d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | G | GTTTTTTT others(2): Show |
6 | a0001c0001t0009g0014 a0001c0001t0009g0022 a0001c0001t0009g0060 others(3): Show |
8 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-3531_287-3523d others(11): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0009g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-3532_287-3523d others(12): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0009g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287-3533_287-3523d others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | G | T | 4 | a0001c0001t0003g0033 a0001c0001t0003g0106 a0001c0001t0003g0116 others(1): Show |
4 | HG04115.hp1 NA18979.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-3552G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479599 | |||||||
| chr15:49479599 | GT | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(45): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.287-3523delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | GTTTTT | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0052 others(5): Show |
10 | HG00609.hp2 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-3527_287-3523d others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | GTTTTTT | G | 59 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(56): Show |
86 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.287-3528_287-3523d others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | GTTTTTTT others(1): Show |
G | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-3530_287-3523d others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479599 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.287-3536_287-3523d others(16): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | ||||||
| chr15:49479612 | T | G | 1 | a0001c0001t0008g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.287-3539T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479612 | |||||||
| chr15:49479780 | A | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-3371A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479780 | |||||||
| chr15:49479810 | C | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3341C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479810 | |||||||
| chr15:49479833 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.287-3318T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479833 | |||||||
| chr15:49479840 | C | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(62): Show |
98 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-3311C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479840 | |||||||
| chr15:49479899 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.287-3252C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479899 | |||||||
| chr15:49479922 | A | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3229A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479922 | |||||||
| chr15:49480040 | T | C | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3111T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480040 | |||||||
| chr15:49480064 | T | C | 1 | a0001c0001t0004g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.287-3087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480064 | |||||||
| chr15:49480071 | T | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3080T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480071 | |||||||
| chr15:49480189 | A | G | 22 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(19): Show |
30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.287-2962A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480189 | |||||||
| chr15:49480393 | T | C | 5 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 others(2): Show |
6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2758T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480393 | |||||||
| chr15:49480474 | A | AT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(152): Show |
230 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.287-2655dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | ||||||
| chr15:49480474 | A | ATT | 20 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0002g0050 others(17): Show |
25 | HG00099.hp2 HG01361.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-2656_287-2655d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | ||||||
| chr15:49480474 | AT | A | 21 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(18): Show |
29 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.287-2655delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | ||||||
| chr15:49480619 | T | C | 3 | a0001c0001t0013g0027 a0001c0001t0013g0076 a0001c0001t0013g0095 |
4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2532T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480619 | |||||||
| chr15:49480706 | T | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2445T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480706 | |||||||
| chr15:49480708 | C | T | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-2443C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480708 | |||||||
| chr15:49480798 | T | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-2353T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480798 | |||||||
| chr15:49480804 | A | G | 1 | a0001c0001t0002g0053 | 2 | HG01928.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.287-2347A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480804 | |||||||
| chr15:49481031 | A | C | 1 | a0001c0001t0002g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287-2120A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481031 | |||||||
| chr15:49481220 | C | T | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1931C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481220 | |||||||
| chr15:49481340 | T | G | 1 | a0001c0001t0015g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.287-1811T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481340 | |||||||
| chr15:49481394 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-1757C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481394 | |||||||
| chr15:49481532 | A | G | 1 | a0001c0001t0007g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.287-1619A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481532 | |||||||
| chr15:49481613 | G | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(228): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.287-1538G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481613 | |||||||
| chr15:49481678 | T | A | 29 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0021 others(26): Show |
40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-1473T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481678 | |||||||
| chr15:49481723 | A | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-1428A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481723 | |||||||
| chr15:49481859 | T | A | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1292T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481859 | |||||||
| chr15:49482148 | G | C | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1003G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482148 | |||||||
| chr15:49482228 | A | C | 23 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(20): Show |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-923A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482228 | |||||||
| chr15:49482284 | G | GAT | 11 | a0001c0001t0006g0004 a0001c0001t0006g0020 a0001c0001t0006g0035 others(8): Show |
21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-859_287-858dup others(2): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49482284 | ||||||
| chr15:49482513 | C | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-638C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482513 | |||||||
| chr15:49482557 | C | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-594C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482557 | |||||||
| chr15:49482766 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
88 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(85): Show |
intron_variant | MODIFIER | c.287-385A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482766 | |||||||
| chr15:49482914 | T | G | 3 | a0001c0001t0015g0043 a0001c0001t0015g0165 a0001c0001t0015g0186 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-237T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482914 | |||||||
| chr15:49482938 | A | AC | 8 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0172 others(5): Show |
10 | HG01169.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-213_287-212ins others(1): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482938 | |||||||
| chr15:49482939 | T | A | 8 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0172 others(5): Show |
10 | HG01169.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-212T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482939 | |||||||
| chr15:49482950 | C | T | 10 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 others(7): Show |
13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-201C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482950 | |||||||
| chr15:49483369 | A | T | 2 | a0001c0001t0015g0043 a0001c0001t0015g0186 |
3 | HG02622.hp2 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.390+115A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483369 | |||||||
| chr15:49483397 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.390+143G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483397 | |||||||
| chr15:49483560 | G | T | 23 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0028 others(20): Show |
31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.390+306G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483560 | |||||||
| chr15:49483832 | T | C | 10 | a0001c0001t0001g0168 a0001c0001t0010g0057 a0001c0001t0010g0231 others(7): Show |
11 | HG00408.hp1 HG01255.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-478T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483832 | |||||||
| chr15:49483922 | C | G | 3 | a0001c0001t0012g0015 a0001c0001t0012g0077 a0001c0001t0012g0079 |
5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-388C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483922 | |||||||
| chr15:49483987 | G | A | 1 | a0001c0001t0014g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-323G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483987 | |||||||
| chr15:49483993 | A | C | 1 | a0001c0001t0011g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-317A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483993 | |||||||
| chr15:49483998 | T | A | 2 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.391-312T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483998 | |||||||
| chr15:49484234 | C | T | 64 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.391-76C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49484234 | |||||||
| chr15:49484292 | G | A | 1 | a0001c0001t0006g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391-18G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49484292 |