Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 197258 |
| ensemblid | ENSG00000157353.17 |
| hgncid | 29500 |
| symbol | FCSK |
| name | fucose kinase |
| refseq_nuc | NM_145059.3 |
| refseq_prot | NP_659496.2 |
| ensembl_nuc | ENST00000288078.11 |
| ensembl_prot | ENSP00000288078.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 70454595 |
| end | 70480274 |
| strand | + |
| ver | v1.2 |
| region | chr16:70454595-70480274 |
| region5000 | chr16:70449595-70485274 |
| regionname0 | FCSK_chr16_70454595_70480274 |
| regionname5000 | FCSK_chr16_70449595_70485274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1084 | 316 | 64 | 71 | 125 | 14 | 40 | 93 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0002 | 0/0 | 1084 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0003 | 0/0 | 1084 | 10 | 0 | 0 | 10 | 0 | 0 | 4 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0004 | 0/0 | 1084 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0005 | 0/0 | 1084 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0006 | 0/0 | 763 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(758): Show |
chr16 | 70449595 | 70485274 |
| a0007 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0008 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0009 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0010 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0011 | 0/0 | 1084 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0012 | 0/0 | 1084 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0013 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0014 | 0/0 | 1084 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0015 | 0/0 | 1084 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0016 | 0/0 | 1084 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(1079): Show |
chr16 | 70449595 | 70485274 |
| a0017 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | MEQPK others(300): Show |
chr16 | 70449595 | 70485274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3252 | 151 | 29 | 25 | 77 | 5 | 14 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0002 | 1/0 | 3252 | 127 | 14 | 37 | 42 | 9 | 24 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0003 | 0/0 | 3252 | 13 | 12 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0006 | 0/0 | 3252 | 9 | 0 | 4 | 5 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0007 | 0/0 | 3252 | 7 | 7 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0009 | 0/0 | 3252 | 4 | 0 | 4 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0010 | 0/0 | 3252 | 2 | 0 | 0 | 0 | 0 | 2 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0016 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0020 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0001c0024 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0002c0004 | 0/0 | 3252 | 11 | 11 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0003c0005 | 0/0 | 3252 | 10 | 0 | 0 | 10 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0004c0008 | 0/0 | 3252 | 4 | 4 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0004c0013 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0005c0011 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0006c0019 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3225): Show |
chr16 | 70449595 | 70485274 | ||
| a0007c0022 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0008c0017 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0009c0026 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0010c0023 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0011c0012 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0012c0027 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0013c0015 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0014c0021 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0015c0014 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0016c0018 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 | ||
| a0017c0025 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | ATGGA others(3247): Show |
chr16 | 70449595 | 70485274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3907 | 150 | 28 | 25 | 77 | 5 | 14 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0001t0004 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0002t0001 | 1/0 | 3907 | 126 | 14 | 37 | 42 | 9 | 23 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0002t0003 | 0/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0003t0001 | 0/0 | 3907 | 13 | 12 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0006t0001 | 0/0 | 3907 | 9 | 0 | 4 | 5 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0007t0001 | 0/0 | 3907 | 7 | 7 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0009t0001 | 0/0 | 3907 | 4 | 0 | 4 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0010t0001 | 0/0 | 3907 | 2 | 0 | 0 | 0 | 0 | 2 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0016t0001 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0020t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0001c0024t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0002c0004t0002 | 0/0 | 3907 | 11 | 11 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0003c0005t0001 | 0/0 | 3907 | 10 | 0 | 0 | 10 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0004c0008t0001 | 0/0 | 3907 | 4 | 4 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0004c0013t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0005c0011t0001 | 0/0 | 3907 | 2 | 2 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0006c0019t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3880): Show |
chr16 | 70449595 | 70485274 |
| a0007c0022t0001 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0008c0017t0001 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0009c0026t0001 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0010c0023t0001 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0011c0012t0002 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0012c0027t0001 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0013c0015t0001 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0014c0021t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0015c0014t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0016c0018t0001 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| a0017c0025t0001 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | AAAGA others(3902): Show |
chr16 | 70449595 | 70485274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 22 | 0 | 5 | 10 | 4 | 2 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 0 | 9 | 0 | 3 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0002 | 0/0 | 14 | 1 | 2 | 8 | 2 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0005 | 1/0 | 7 | 0 | 5 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0006 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0007 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0013 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0006t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0006t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0009t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0010t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0016t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0020t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0001c0024t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0002c0004t0002g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0002c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0002c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0002c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0003c0005t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0003c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0004c0008t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0004c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0004c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0004c0013t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0005c0011t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0006c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0007c0022t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0008c0017t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0009c0026t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0010c0023t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0011c0012t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0012c0027t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0013c0015t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0014c0021t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0015c0014t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0016c0018t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| a0017c0025t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | GBR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | GBR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0112 | EUR | FIN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0009 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00558 | hp2 | a0003 | c0005 | t0001 | g0009 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00597 | hp1 | a0006 | c0019 | t0001 | g0001 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00642 | hp1 | a0007 | c0022 | t0001 | g0030 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01070 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0002 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01071 | hp2 | a0001 | c0009 | t0001 | g0002 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01169 | hp2 | a0008 | c0017 | t0001 | g0044 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01257 | hp1 | a0001 | c0009 | t0001 | g0002 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01258 | hp2 | a0001 | c0009 | t0001 | g0002 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01346 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01346 | hp2 | a0009 | c0026 | t0001 | g0010 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01361 | hp2 | a0010 | c0023 | t0001 | g0091 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01884 | hp2 | a0005 | c0011 | t0001 | g0026 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01891 | hp1 | a0011 | c0012 | t0002 | g0004 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01891 | hp2 | a0004 | c0008 | t0001 | g0051 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01943 | hp1 | a0001 | c0006 | t0001 | g0022 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01981 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02074 | hp1 | a0012 | c0027 | t0001 | g0069 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02080 | hp1 | a0003 | c0005 | t0001 | g0163 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02083 | hp1 | a0003 | c0005 | t0001 | g0160 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02083 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02132 | hp1 | a0003 | c0005 | t0001 | g0009 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02148 | hp1 | a0013 | c0015 | t0001 | g0021 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CDX | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02280 | hp1 | a0002 | c0004 | t0002 | g0046 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02451 | hp1 | a0002 | c0004 | t0002 | g0048 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02451 | hp2 | a0001 | c0007 | t0001 | g0043 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02630 | hp1 | a0014 | c0021 | t0001 | g0008 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0025 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02723 | hp1 | a0001 | c0007 | t0001 | g0038 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02723 | hp2 | a0015 | c0014 | t0001 | g0052 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02809 | hp2 | a0004 | c0008 | t0001 | g0027 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02886 | hp1 | a0002 | c0004 | t0002 | g0004 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02922 | hp1 | a0002 | c0004 | t0002 | g0004 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02965 | hp1 | a0004 | c0008 | t0001 | g0049 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03098 | hp2 | a0002 | c0004 | t0002 | g0004 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03130 | hp2 | a0004 | c0008 | t0001 | g0027 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03195 | hp2 | a0002 | c0004 | t0002 | g0004 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03453 | hp1 | a0002 | c0004 | t0002 | g0047 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03453 | hp2 | a0002 | c0004 | t0002 | g0004 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03486 | hp1 | a0002 | c0004 | t0002 | g0004 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03486 | hp2 | a0001 | c0007 | t0001 | g0039 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03490 | hp1 | a0001 | c0010 | t0001 | g0005 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03492 | hp2 | a0001 | c0010 | t0001 | g0005 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0120 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | STU | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18612 | hp2 | a0003 | c0005 | t0001 | g0009 | EAS | CHB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | YRI | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18906 | hp2 | a0002 | c0004 | t0002 | g0004 | AFR | YRI | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18945 | hp1 | a0003 | c0005 | t0001 | g0009 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18959 | hp1 | a0001 | c0006 | t0001 | g0023 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18962 | hp2 | a0003 | c0005 | t0001 | g0009 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18974 | hp2 | a0016 | c0018 | t0001 | g0189 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18994 | hp2 | a0001 | c0006 | t0001 | g0022 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19009 | hp1 | a0003 | c0005 | t0001 | g0161 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19009 | hp2 | a0001 | c0016 | t0001 | g0022 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19012 | hp1 | a0003 | c0005 | t0001 | g0009 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19012 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | LWK | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19030 | hp2 | a0017 | c0025 | t0001 | g0108 | AFR | LWK | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0140 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20129 | hp1 | a0001 | c0024 | t0001 | g0014 | AFR | ASW | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ASW | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0094 | EUR | TSI | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | GIH | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02109 | hp1 | a0002 | c0004 | t0002 | g0004 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02109 | hp2 | a0001 | c0007 | t0001 | g0041 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02486 | hp2 | a0001 | c0007 | t0001 | g0040 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG02559 | hp2 | a0001 | c0020 | t0001 | g0035 | AFR | ACB | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG06807 | hp1 | a0004 | c0013 | t0001 | g0050 | AFR | USA | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | USA | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | USA | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| NA21309 | hp2 | a0005 | c0011 | t0001 | g0026 | AFR | LWK | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0005 | REF | REF | FCSK_chr16_70449595_70485274 | FCSK | chr16 | 70449595 | 70485274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70463701 | T | G | 1 | a0013 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.161T>G | p.Val54Gly | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/24 | 219/3907 | 161/3255 | 54/1084 | chr16 | 70463701 | |||
| chr16:70466181 | C | T | 1 | a0012 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.335C>T | p.Pro112Leu | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 5/24 | 393/3907 | 335/3255 | 112/1084 | chr16 | 70466181 | |||
| chr16:70469192 | A | G | 1 | a0009 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.824A>G | p.Asn275Ser | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/24 | 882/3907 | 824/3255 | 275/1084 | chr16 | 70469192 | |||
| chr16:70469284 | C | T | 1 | a0017 | 1 | NA19030.hp2 | stop_gained | HIGH | c.916C>T | p.Gln306* | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/24 | 974/3907 | 916/3255 | 306/1084 | chr16 | 70469284 | |||
| chr16:70471336 | G | T | 1 | a0015 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1325G>T | p.Arg442Leu | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/24 | 1383/3907 | 1325/3255 | 442/1084 | chr16 | 70471336 | |||
| chr16:70472605 | G | A | 1 | a0008 | 1 | HG01169.hp2 | missense_variant&splice_region_variant | MODERATE | c.1406G>A | p.Arg469Gln | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 14/24 | 1464/3907 | 1406/3255 | 469/1084 | chr16 | 70472605 | |||
| chr16:70473137 | G | A | 2 | a0002 a0011 |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
missense_variant | MODERATE | c.1561G>A | p.Ala521Thr | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/24 | 1619/3907 | 1561/3255 | 521/1084 | chr16 | 70473137 | |||
| chr16:70473180 | C | T | 1 | a0014 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1604C>T | p.Pro535Leu | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/24 | 1662/3907 | 1604/3255 | 535/1084 | chr16 | 70473180 | |||
| chr16:70473279 | T | G | 1 | a0016 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.1703T>G | p.Leu568Arg | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/24 | 1761/3907 | 1703/3255 | 568/1084 | chr16 | 70473279 | |||
| chr16:70473288 | G | A | 1 | a0005 | 2 | HG01884.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1712G>A | p.Arg571His | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/24 | 1770/3907 | 1712/3255 | 571/1084 | chr16 | 70473288 | |||
| chr16:70474622 | ACAGAGCA others(15): Show |
A | 1 | a0006 | 1 | HG00597.hp1 | frameshift_variant | HIGH | c.2084_2105delCAGAGC others(16): Show |
p.Thr695fs | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 17/24 | 2142/3907 | 2084/3255 | 695/1084 | chr16 | 70474622 | |||
| chr16:70475698 | G | A | 1 | a0007 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.2572G>A | p.Ala858Thr | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/24 | 2630/3907 | 2572/3255 | 858/1084 | chr16 | 70475698 | |||
| chr16:70475707 | G | A | 2 | a0004 a0015 |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.2581G>A | p.Val861Met | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/24 | 2639/3907 | 2581/3255 | 861/1084 | chr16 | 70475707 | |||
| chr16:70478445 | C | T | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2815C>T | p.Arg939Trp | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 21/24 | 2873/3907 | 2815/3255 | 939/1084 | chr16 | 70478445 | |||
| chr16:70478607 | C | A | 1 | a0003 | 10 | HG00423.hp2 HG00558.hp2 HG02080.hp1 others(7): Show |
missense_variant | MODERATE | c.2886C>A | p.Ser962Arg | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/24 | 2944/3907 | 2886/3255 | 962/1084 | chr16 | 70478607 | |||
| chr16:70479293 | C | A | 1 | a0010 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.3043C>A | p.His1015Asn | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 23/24 | 3101/3907 | 3043/3255 | 1015/1084 | chr16 | 70479293 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70463202 | G | A | 2 | a0002c0004 a0011c0012 |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.12G>A | p.Pro4Pro | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 2/24 | 70/3907 | 12/3255 | 4/1084 | chr16 | 70463202 | |||
| chr16:70463678 | C | A | 4 | a0001c0003 a0004c0008 a0004c0013 others(1): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
synonymous_variant | LOW | c.138C>A | p.Ala46Ala | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/24 | 196/3907 | 138/3255 | 46/1084 | chr16 | 70463678 | |||
| chr16:70466167 | T | C | 6 | a0001c0003 a0002c0004 a0004c0008 others(3): Show |
31 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
synonymous_variant | LOW | c.321T>C | p.Ala107Ala | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 5/24 | 379/3907 | 321/3255 | 107/1084 | chr16 | 70466167 | |||
| chr16:70467411 | C | T | 1 | a0001c0006 | 9 | HG01070.hp1 HG01346.hp1 HG01943.hp1 others(6): Show |
synonymous_variant | LOW | c.522C>T | p.Ile174Ile | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/24 | 580/3907 | 522/3255 | 174/1084 | chr16 | 70467411 | |||
| chr16:70468944 | G | A | 2 | a0002c0004 a0011c0012 |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.759G>A | p.Leu253Leu | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 9/24 | 817/3907 | 759/3255 | 253/1084 | chr16 | 70468944 | |||
| chr16:70469172 | T | A | 1 | a0001c0010 | 2 | HG03490.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.804T>A | p.Ile268Ile | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/24 | 862/3907 | 804/3255 | 268/1084 | chr16 | 70469172 | |||
| chr16:70470402 | C | G | 1 | a0001c0009 | 4 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(1): Show |
synonymous_variant | LOW | c.1044C>G | p.Ala348Ala | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 11/24 | 1102/3907 | 1044/3255 | 348/1084 | chr16 | 70470402 | |||
| chr16:70470982 | T | C | 7 | a0001c0003 a0001c0007 a0002c0004 others(4): Show |
38 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(35): Show |
synonymous_variant | LOW | c.1080T>C | p.Leu360Leu | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 12/24 | 1138/3907 | 1080/3255 | 360/1084 | chr16 | 70470982 | |||
| chr16:70471310 | G | A | 1 | a0001c0016 | 1 | NA19009.hp2 | synonymous_variant | LOW | c.1299G>A | p.Pro433Pro | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/24 | 1357/3907 | 1299/3255 | 433/1084 | chr16 | 70471310 | |||
| chr16:70473004 | T | C | 18 | a0001c0001 a0001c0003 a0001c0006 others(15): Show |
216 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
synonymous_variant | LOW | c.1428T>C | p.Pro476Pro | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/24 | 1486/3907 | 1428/3255 | 476/1084 | chr16 | 70473004 | |||
| chr16:70474642 | G | A | 2 | a0002c0004 a0011c0012 |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.2103G>A | p.Pro701Pro | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 17/24 | 2161/3907 | 2103/3255 | 701/1084 | chr16 | 70474642 | |||
| chr16:70474875 | C | T | 1 | a0001c0024 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2241C>T | p.Pro747Pro | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 18/24 | 2299/3907 | 2241/3255 | 747/1084 | chr16 | 70474875 | |||
| chr16:70478288 | C | T | 5 | a0001c0003 a0002c0004 a0004c0008 others(2): Show |
30 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
synonymous_variant | LOW | c.2658C>T | p.Asp886Asp | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 21/24 | 2716/3907 | 2658/3255 | 886/1084 | chr16 | 70478288 | |||
| chr16:70479280 | T | C | 1 | a0001c0020 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.3030T>C | p.Asp1010Asp | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 23/24 | 3088/3907 | 3030/3255 | 1010/1084 | chr16 | 70479280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70463183 | T | G | 2 | a0002c0004t0002 a0011c0012t0002 |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-8T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 2/24 | chr16 | 70463183 | |||||||
| chr16:70479954 | C | A | 1 | a0001c0002t0003 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 24/24 | 274 | chr16 | 70479954 | ||||||
| chr16:70479999 | T | A | 1 | a0001c0001t0004 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319T>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 24/24 | 319 | chr16 | 70479999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70454657 | A | AGCGCCCC others(2): Show |
6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+53_-23+61dupTT others(7): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454657 | ||||||
| chr16:70454657 | A | AGCGCCCC others(11): Show |
21 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0024 others(18): Show |
32 | HG00597.hp2 HG00733.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.-23+44_-23+61dupTT others(16): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454657 | ||||||
| chr16:70454657 | A | AGCGCCCC others(20): Show |
1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-23+35_-23+61dupTT others(25): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454657 | ||||||
| chr16:70454657 | A | AGCGCCCC others(38): Show |
1 | a0001c0001t0001g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-23+61_-23+62insTT others(43): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454657 | ||||||
| chr16:70454657 | AGCGCCCC others(2): Show |
A | 9 | a0001c0002t0001g0042 a0001c0007t0001g0025 a0001c0007t0001g0038 others(6): Show |
11 | HG01169.hp2 HG01884.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+53_-23+61delTT others(7): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454657 | ||||||
| chr16:70454674 | T | TTGCGCCC others(2): Show |
16 | a0001c0003t0001g0045 a0001c0003t0001g0053 a0001c0003t0001g0054 others(13): Show |
24 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-23+52_-23+53insCT others(7): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454674 | ||||||
| chr16:70454683 | T | C | 16 | a0001c0003t0001g0045 a0001c0003t0001g0053 a0001c0003t0001g0054 others(13): Show |
24 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-23+53T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454683 | |||||||
| chr16:70454683 | T | TTGCGCCC others(11): Show |
2 | a0001c0003t0001g0011 a0001c0003t0001g0171 |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+63_-23+64insGC others(16): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454683 | ||||||
| chr16:70454688 | C | CCCCTTGC others(10): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | NA18961.hp2 NA18980.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-23+61_-23+62insTT others(15): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454688 | ||||||
| chr16:70454709 | C | T | 1 | a0001c0002t0001g0037 | 2 | HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-23+79C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454709 | |||||||
| chr16:70454716 | T | TGACTGGG others(6): Show |
1 | a0001c0003t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-23+89_-23+101dupC others(12): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70454716 | ||||||
| chr16:70454829 | T | C | 18 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(15): Show |
31 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+199T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454829 | |||||||
| chr16:70454861 | A | C | 1 | a0001c0001t0004g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-23+231A>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454861 | |||||||
| chr16:70454896 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0058 |
3 | NA18940.hp1 NA18943.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-23+266G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454896 | |||||||
| chr16:70454925 | C | T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+295C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454925 | |||||||
| chr16:70454966 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-23+336T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70454966 | |||||||
| chr16:70455014 | G | A | 4 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): Show |
8 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+384G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455014 | |||||||
| chr16:70455272 | G | C | 1 | a0001c0002t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-23+642G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455272 | |||||||
| chr16:70455355 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-23+725C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455355 | |||||||
| chr16:70455479 | C | CG | 4 | a0001c0001t0001g0063 a0001c0002t0001g0016 a0001c0002t0001g0064 others(1): Show |
7 | HG00639.hp2 HG01123.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+850dupG | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70455479 | ||||||
| chr16:70455504 | C | CCAA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(69): Show |
127 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-23+890_-23+892dup others(3): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70455504 | ||||||
| chr16:70455522 | A | AC | 4 | a0001c0001t0001g0023 a0001c0002t0001g0167 a0001c0002t0001g0168 others(1): Show |
5 | NA18947.hp1 NA18947.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+892_-23+893ins others(1): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455522 | |||||||
| chr16:70455595 | T | TA | 9 | a0001c0001t0001g0123 a0001c0001t0001g0178 a0001c0007t0001g0038 others(6): Show |
16 | HG01891.hp1 HG02109.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+979dupA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70455595 | ||||||
| chr16:70455676 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-23+1046A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455676 | |||||||
| chr16:70455734 | A | C | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+1104A>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455734 | |||||||
| chr16:70455846 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-23+1216C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455846 | |||||||
| chr16:70455888 | C | CA | 11 | a0001c0001t0001g0066 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
18 | HG01433.hp2 HG01891.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+1271dupA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70455888 | ||||||
| chr16:70455909 | A | T | 1 | a0001c0003t0001g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-23+1279A>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455909 | |||||||
| chr16:70455990 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-23+1360C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70455990 | |||||||
| chr16:70456007 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-23+1377G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456007 | |||||||
| chr16:70456018 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+1388A>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456018 | |||||||
| chr16:70456143 | C | T | 1 | a0002c0004t0002g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-23+1513C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456143 | |||||||
| chr16:70456160 | C | T | 1 | a0001c0007t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-23+1530C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456160 | |||||||
| chr16:70456618 | A | C | 6 | a0001c0001t0001g0165 a0002c0004t0002g0004 a0002c0004t0002g0046 others(3): Show |
13 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+1988A>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456618 | |||||||
| chr16:70456643 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-23+2013T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456643 | |||||||
| chr16:70456808 | C | G | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+2178C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70456808 | |||||||
| chr16:70457019 | TA | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0157 others(13): Show |
33 | HG00423.hp2 HG00558.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.-23+2400delA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70457019 | ||||||
| chr16:70457189 | A | T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+2559A>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457189 | |||||||
| chr16:70457201 | C | T | 1 | a0001c0002t0003g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-23+2571C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457201 | |||||||
| chr16:70457264 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-23+2634T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457264 | |||||||
| chr16:70457286 | G | T | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.-23+2656G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457286 | |||||||
| chr16:70457315 | C | T | 6 | a0001c0001t0001g0165 a0002c0004t0002g0004 a0002c0004t0002g0046 others(3): Show |
13 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+2685C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457315 | |||||||
| chr16:70457401 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0117 a0001c0001t0001g0191 |
8 | HG00733.hp2 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+2771C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457401 | |||||||
| chr16:70457415 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-23+2785C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457415 | |||||||
| chr16:70457564 | GTTTC | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+2958_-23+2961d others(6): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70457564 | ||||||
| chr16:70457564 | GTTTCTTT others(5): Show |
G | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-23+2950_-23+2961d others(14): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70457564 | ||||||
| chr16:70457621 | C | T | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+2991C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457621 | |||||||
| chr16:70457727 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-23+3097C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457727 | |||||||
| chr16:70457752 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-23+3122G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457752 | |||||||
| chr16:70457764 | GT | G | 41 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(38): Show |
63 | HG00738.hp2 HG01243.hp1 HG01433.hp2 others(60): Show |
intron_variant | MODIFIER | c.-23+3147delT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70457764 | ||||||
| chr16:70457824 | T | G | 1 | a0012c0027t0001g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-23+3194T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457824 | |||||||
| chr16:70457840 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+3210G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457840 | |||||||
| chr16:70457889 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-23+3259A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457889 | |||||||
| chr16:70457959 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-23+3329G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70457959 | |||||||
| chr16:70458077 | TA | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+3459delA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70458077 | ||||||
| chr16:70458077 | TAA | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-23+3458_-23+3459d others(4): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70458077 | ||||||
| chr16:70458163 | C | CT | 7 | a0001c0001t0001g0156 a0001c0001t0001g0164 a0004c0008t0001g0027 others(4): Show |
8 | HG01891.hp2 HG02040.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+3547dupT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70458163 | ||||||
| chr16:70458218 | G | A | 1 | a0001c0002t0001g0070 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-23+3588G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458218 | |||||||
| chr16:70458362 | G | A | 1 | a0001c0006t0001g0140 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-23+3732G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458362 | |||||||
| chr16:70458363 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-23+3733C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458363 | |||||||
| chr16:70458364 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-23+3734T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458364 | |||||||
| chr16:70458532 | T | A | 1 | a0001c0002t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-23+3902T>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458532 | |||||||
| chr16:70458545 | C | A | 6 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(3): Show |
6 | NA18953.hp1 NA18966.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+3915C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458545 | |||||||
| chr16:70458605 | T | G | 1 | a0001c0002t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-23+3975T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458605 | |||||||
| chr16:70458833 | T | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(16): Show |
34 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-23+4203T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458833 | |||||||
| chr16:70458966 | A | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-4203A>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70458966 | |||||||
| chr16:70459028 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-4141T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459028 | |||||||
| chr16:70459084 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-4085A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459084 | |||||||
| chr16:70459223 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-22-3946T>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459223 | |||||||
| chr16:70459223 | TA | T | 24 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0155 others(21): Show |
30 | HG00323.hp1 HG01256.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-22-3930delA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70459223 | ||||||
| chr16:70459223 | TAA | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(17): Show |
35 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-22-3931_-22-3930d others(4): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70459223 | ||||||
| chr16:70459382 | C | T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-3787C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459382 | |||||||
| chr16:70459539 | G | A | 36 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(33): Show |
57 | HG00738.hp2 HG01243.hp1 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.-22-3630G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459539 | |||||||
| chr16:70459635 | C | G | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-3534C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459635 | |||||||
| chr16:70459653 | C | T | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-3516C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459653 | |||||||
| chr16:70459656 | C | CT | 37 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(34): Show |
53 | HG00738.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.-22-3494dupT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70459656 | ||||||
| chr16:70459732 | C | T | 4 | a0003c0005t0001g0009 a0003c0005t0001g0160 a0003c0005t0001g0161 others(1): Show |
10 | HG00423.hp2 HG00558.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22-3437C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459732 | |||||||
| chr16:70459803 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-22-3366A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459803 | |||||||
| chr16:70459805 | CT | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(19): Show |
37 | HG00738.hp2 HG01243.hp1 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22-3352delT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70459805 | ||||||
| chr16:70459811 | T | C | 1 | a0001c0003t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-22-3358T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459811 | |||||||
| chr16:70459903 | G | C | 1 | a0001c0002t0001g0076 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-22-3266G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459903 | |||||||
| chr16:70459988 | G | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-3181G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70459988 | |||||||
| chr16:70460056 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-3113C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460056 | |||||||
| chr16:70460060 | A | G | 16 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0020 others(13): Show |
41 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-22-3109A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460060 | |||||||
| chr16:70460086 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-3083G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460086 | |||||||
| chr16:70460104 | C | CT | 8 | a0001c0001t0001g0033 a0001c0001t0001g0151 a0001c0001t0001g0159 others(5): Show |
9 | HG01175.hp2 HG01361.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-3045dupT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70460104 | ||||||
| chr16:70460104 | C | CTT | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-3046_-22-3045d others(4): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70460104 | ||||||
| chr16:70460104 | CT | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0141 a0001c0001t0001g0164 others(6): Show |
10 | HG01433.hp1 HG02040.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22-3045delT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70460104 | ||||||
| chr16:70460104 | CTTTT | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-3048_-22-3045d others(6): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70460104 | ||||||
| chr16:70460145 | C | T | 4 | a0001c0002t0001g0079 a0001c0002t0001g0100 a0001c0002t0001g0101 others(1): Show |
4 | HG01109.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-3024C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460145 | |||||||
| chr16:70460172 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-22-2997C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460172 | |||||||
| chr16:70460205 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22-2964G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460205 | |||||||
| chr16:70460226 | C | G | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-2943C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460226 | |||||||
| chr16:70460240 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-22-2929T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460240 | |||||||
| chr16:70460333 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-22-2836G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460333 | |||||||
| chr16:70460346 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(31): Show |
55 | HG00738.hp2 HG01243.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.-22-2823T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460346 | |||||||
| chr16:70460362 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-22-2807C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460362 | |||||||
| chr16:70460495 | C | T | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-2674C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460495 | |||||||
| chr16:70460529 | T | C | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2640T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460529 | |||||||
| chr16:70460530 | G | A | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2639G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460530 | |||||||
| chr16:70460540 | G | A | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2629G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460540 | |||||||
| chr16:70460542 | C | T | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2627C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460542 | |||||||
| chr16:70460549 | C | T | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2620C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460549 | |||||||
| chr16:70460550 | A | G | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2619A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460550 | |||||||
| chr16:70460551 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-22-2618C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460551 | |||||||
| chr16:70460552 | G | C | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2617G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460552 | |||||||
| chr16:70460553 | T | C | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2616T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460553 | |||||||
| chr16:70460554 | G | A | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2615G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460554 | |||||||
| chr16:70460570 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-2599A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460570 | |||||||
| chr16:70460577 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-2592G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460577 | |||||||
| chr16:70460586 | T | G | 1 | a0001c0007t0001g0025 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-2583T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460586 | |||||||
| chr16:70460593 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-2576C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460593 | |||||||
| chr16:70460625 | A | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(31): Show |
55 | HG00738.hp2 HG01243.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.-22-2544A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460625 | |||||||
| chr16:70460978 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-2191G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70460978 | |||||||
| chr16:70461041 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-2128G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461041 | |||||||
| chr16:70461090 | A | AGGCGGGC others(335): Show |
1 | a0001c0001t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-22-2075_-22-2074i others(344): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70461090 | ||||||
| chr16:70461175 | C | A | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-1994C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461175 | |||||||
| chr16:70461213 | G | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(16): Show |
31 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.-22-1956G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461213 | |||||||
| chr16:70461362 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-22-1807T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461362 | |||||||
| chr16:70461389 | C | T | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-1780C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461389 | |||||||
| chr16:70461396 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-22-1773G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461396 | |||||||
| chr16:70461526 | T | G | 2 | a0001c0003t0001g0011 a0001c0003t0001g0171 |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-1643T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461526 | |||||||
| chr16:70461620 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-1549C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461620 | |||||||
| chr16:70461686 | T | TG | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-1477dupG | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70461686 | ||||||
| chr16:70461868 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-22-1301C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461868 | |||||||
| chr16:70461882 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0082 others(36): Show |
61 | HG00738.hp2 HG01243.hp1 HG01433.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22-1287G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461882 | |||||||
| chr16:70461902 | T | C | 5 | a0001c0003t0001g0053 a0001c0007t0001g0025 a0001c0007t0001g0040 others(2): Show |
6 | HG01433.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-1267T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70461902 | |||||||
| chr16:70462008 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-1161C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462008 | |||||||
| chr16:70462146 | C | CTTATT | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-1021_-22-1020i others(7): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | 70462146 | ||||||
| chr16:70462150 | T | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-1019T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462150 | |||||||
| chr16:70462224 | T | C | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-945T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462224 | |||||||
| chr16:70462385 | A | G | 25 | a0001c0001t0001g0098 a0001c0003t0001g0011 a0001c0003t0001g0045 others(22): Show |
39 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22-784A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462385 | |||||||
| chr16:70462390 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-22-779G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462390 | |||||||
| chr16:70462470 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-22-699C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462470 | |||||||
| chr16:70462515 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-22-654G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462515 | |||||||
| chr16:70462545 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-22-624C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462545 | |||||||
| chr16:70462548 | A | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-621A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462548 | |||||||
| chr16:70462630 | C | T | 24 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(21): Show |
38 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.-22-539C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462630 | |||||||
| chr16:70462778 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(66): Show |
125 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-22-391G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462778 | |||||||
| chr16:70462835 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-334G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462835 | |||||||
| chr16:70462891 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-22-278C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462891 | |||||||
| chr16:70462924 | C | T | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-245C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462924 | |||||||
| chr16:70462942 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-22-227G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70462942 | |||||||
| chr16:70463066 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-103G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 1/23 | chr16 | 70463066 | |||||||
| chr16:70463332 | A | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+60A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 2/23 | chr16 | 70463332 | |||||||
| chr16:70463345 | A | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+73A>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 2/23 | chr16 | 70463345 | |||||||
| chr16:70463563 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0078 |
3 | HG00099.hp2 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.83-60C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 2/23 | chr16 | 70463563 | |||||||
| chr16:70463865 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.234+91T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70463865 | |||||||
| chr16:70463950 | G | GGCAGGGC others(318): Show |
3 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0013t0001g0050 |
4 | HG02809.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+191_234+192ins others(325): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70463950 | ||||||
| chr16:70463950 | G | GGCAGGGC others(319): Show |
1 | a0004c0008t0001g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.234+191_234+192ins others(326): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70463950 | ||||||
| chr16:70463950 | G | GGCAGGGC others(319): Show |
4 | a0001c0003t0001g0011 a0001c0003t0001g0053 a0001c0003t0001g0054 others(1): Show |
9 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+191_234+192ins others(326): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70463950 | ||||||
| chr16:70463950 | G | GGCAGGGC others(320): Show |
4 | a0001c0003t0001g0045 a0001c0003t0001g0056 a0001c0003t0001g0057 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+191_234+192ins others(327): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70463950 | ||||||
| chr16:70463950 | G | GGCAGGGC others(318): Show |
1 | a0015c0014t0001g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+186_234+187ins others(325): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70463950 | ||||||
| chr16:70463986 | T | G | 20 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(17): Show |
33 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.234+212T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70463986 | |||||||
| chr16:70464015 | G | A | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+241G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464015 | |||||||
| chr16:70464220 | C | T | 24 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(21): Show |
38 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.234+446C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464220 | |||||||
| chr16:70464374 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.234+600G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464374 | |||||||
| chr16:70464588 | GTTGCAGT others(17): Show |
G | 18 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(15): Show |
31 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.235-484_235-461del others(24): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70464588 | ||||||
| chr16:70464699 | C | CA | 31 | a0001c0001t0001g0128 a0001c0001t0001g0142 a0001c0001t0001g0143 others(28): Show |
39 | HG00323.hp1 HG01261.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.235-406dupA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70464699 | ||||||
| chr16:70464699 | CA | C | 12 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0079 others(9): Show |
19 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.235-406delA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | 70464699 | ||||||
| chr16:70464719 | A | G | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-407A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464719 | |||||||
| chr16:70464847 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.235-279C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464847 | |||||||
| chr16:70464871 | C | T | 1 | a0004c0013t0001g0050 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235-255C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464871 | |||||||
| chr16:70464990 | C | G | 1 | a0001c0002t0001g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235-136C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 3/23 | chr16 | 70464990 | |||||||
| chr16:70465379 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0076 a0001c0002t0001g0104 others(1): Show |
11 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+203C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 4/23 | chr16 | 70465379 | |||||||
| chr16:70465528 | C | T | 1 | a0001c0007t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.285+352C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 4/23 | chr16 | 70465528 | |||||||
| chr16:70465671 | C | T | 6 | a0001c0003t0001g0011 a0001c0003t0001g0053 a0001c0003t0001g0054 others(3): Show |
11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-461C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 4/23 | chr16 | 70465671 | |||||||
| chr16:70465824 | A | G | 2 | a0001c0007t0001g0025 a0001c0007t0001g0040 |
3 | HG02486.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-308A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 4/23 | chr16 | 70465824 | |||||||
| chr16:70466097 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.286-35C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 4/23 | chr16 | 70466097 | |||||||
| chr16:70466542 | A | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.411+285A>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 5/23 | chr16 | 70466542 | |||||||
| chr16:70466605 | G | A | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-277G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 5/23 | chr16 | 70466605 | |||||||
| chr16:70466693 | G | A | 1 | a0003c0005t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.412-189G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 5/23 | chr16 | 70466693 | |||||||
| chr16:70467051 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.484+97C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467051 | |||||||
| chr16:70467066 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.484+112C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467066 | |||||||
| chr16:70467230 | C | T | 1 | a0001c0002t0001g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.485-144C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467230 | |||||||
| chr16:70467247 | T | C | 1 | a0017c0025t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-127T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467247 | |||||||
| chr16:70467323 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.485-51C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467323 | |||||||
| chr16:70467352 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485-22T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 6/23 | chr16 | 70467352 | |||||||
| chr16:70467487 | A | G | 6 | a0001c0001t0001g0165 a0002c0004t0002g0004 a0002c0004t0002g0046 others(3): Show |
13 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.582+16A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467487 | |||||||
| chr16:70467497 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0004g0170 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.582+26C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467497 | |||||||
| chr16:70467540 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.582+69T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467540 | |||||||
| chr16:70467562 | C | T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.582+91C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467562 | |||||||
| chr16:70467618 | A | G | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.582+147A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467618 | |||||||
| chr16:70467630 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.582+159C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467630 | |||||||
| chr16:70467680 | C | T | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-206C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467680 | |||||||
| chr16:70467858 | C | T | 1 | a0001c0002t0001g0019 | 3 | HG02165.hp2 NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.583-28C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 7/23 | chr16 | 70467858 | |||||||
| chr16:70468027 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.663+61T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468027 | |||||||
| chr16:70468037 | T | G | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+71T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468037 | |||||||
| chr16:70468361 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.663+395G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468361 | |||||||
| chr16:70468590 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.664-259G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468590 | |||||||
| chr16:70468610 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.664-239C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468610 | |||||||
| chr16:70468666 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.664-183G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468666 | |||||||
| chr16:70468707 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(129): Show |
219 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.664-142C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468707 | |||||||
| chr16:70468732 | C | T | 3 | a0001c0002t0001g0084 a0001c0002t0001g0114 a0010c0023t0001g0091 |
3 | HG01256.hp1 HG01361.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.664-117C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468732 | |||||||
| chr16:70468735 | C | G | 1 | a0001c0002t0001g0090 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.664-114C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468735 | |||||||
| chr16:70468781 | C | T | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-68C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468781 | |||||||
| chr16:70468813 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.664-36G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 8/23 | chr16 | 70468813 | |||||||
| chr16:70468984 | C | G | 1 | a0001c0002t0001g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.783+16C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 9/23 | chr16 | 70468984 | |||||||
| chr16:70469073 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.784-79G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 9/23 | chr16 | 70469073 | |||||||
| chr16:70469491 | C | G | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.955+168C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469491 | |||||||
| chr16:70469516 | C | T | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.955+193C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469516 | |||||||
| chr16:70469554 | T | A | 2 | a0001c0007t0001g0041 a0001c0007t0001g0043 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.955+231T>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469554 | |||||||
| chr16:70469597 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.955+274C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469597 | |||||||
| chr16:70469813 | A | G | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+490A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469813 | |||||||
| chr16:70469837 | C | T | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.956-477C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469837 | |||||||
| chr16:70469914 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.956-400G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70469914 | |||||||
| chr16:70470064 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(65): Show |
124 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.956-250C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70470064 | |||||||
| chr16:70470138 | C | T | 2 | a0001c0003t0001g0054 a0001c0003t0001g0055 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.956-176C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70470138 | |||||||
| chr16:70470145 | C | G | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-169C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 10/23 | chr16 | 70470145 | |||||||
| chr16:70470597 | G | C | 5 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+171G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 11/23 | chr16 | 70470597 | |||||||
| chr16:70470674 | T | C | 1 | a0001c0002t0001g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1068+248T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 11/23 | chr16 | 70470674 | |||||||
| chr16:70470937 | ACCC | A | 14 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(11): Show |
23 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1069-30_1069-28del others(3): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr16 | 70470937 | ||||||
| chr16:70471111 | C | T | 1 | a0001c0003t0001g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1170+39C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 12/23 | chr16 | 70471111 | |||||||
| chr16:70471433 | G | C | 1 | a0001c0001t0004g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1341+81G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70471433 | |||||||
| chr16:70471493 | G | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0126 others(9): Show |
29 | HG00423.hp2 HG00558.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.1341+141G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70471493 | |||||||
| chr16:70471812 | G | GT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(43): Show |
67 | HG00609.hp2 HG00738.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1341+477dupT | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr16 | 70471812 | ||||||
| chr16:70471854 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1341+502G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70471854 | |||||||
| chr16:70471950 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1342-591C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70471950 | |||||||
| chr16:70472008 | C | T | 9 | a0001c0001t0001g0186 a0001c0003t0001g0011 a0001c0003t0001g0045 others(6): Show |
14 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1342-533C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472008 | |||||||
| chr16:70472045 | C | A | 1 | a0001c0002t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1342-496C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472045 | |||||||
| chr16:70472100 | C | T | 1 | a0002c0004t0002g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1342-441C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472100 | |||||||
| chr16:70472109 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1342-432G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472109 | |||||||
| chr16:70472160 | G | C | 1 | a0001c0003t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1342-381G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472160 | |||||||
| chr16:70472199 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1342-342G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472199 | |||||||
| chr16:70472238 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1342-303C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472238 | |||||||
| chr16:70472286 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1342-255A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472286 | |||||||
| chr16:70472315 | T | C | 6 | a0001c0007t0001g0025 a0001c0007t0001g0038 a0001c0007t0001g0039 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1342-226T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472315 | |||||||
| chr16:70472480 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1342-61G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 13/23 | chr16 | 70472480 | |||||||
| chr16:70472654 | G | A | 21 | a0001c0001t0001g0098 a0001c0001t0004g0170 a0001c0003t0001g0011 others(18): Show |
28 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1406+49G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 14/23 | chr16 | 70472654 | |||||||
| chr16:70472766 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1406+161C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 14/23 | chr16 | 70472766 | |||||||
| chr16:70472849 | C | T | 18 | a0001c0001t0001g0148 a0001c0002t0001g0010 a0001c0002t0001g0042 others(15): Show |
22 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.1407-134C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 14/23 | chr16 | 70472849 | |||||||
| chr16:70472901 | G | C | 2 | a0001c0003t0001g0054 a0001c0003t0001g0055 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1407-82G>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 14/23 | chr16 | 70472901 | |||||||
| chr16:70473390 | CA | C | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1777+38delA | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473390 | |||||||
| chr16:70473734 | G | T | 3 | a0001c0002t0001g0084 a0001c0002t0001g0114 a0010c0023t0001g0091 |
3 | HG01256.hp1 HG01361.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1777+381G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473734 | |||||||
| chr16:70473773 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1778-356G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473773 | |||||||
| chr16:70473802 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1778-327T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473802 | |||||||
| chr16:70473870 | A | G | 2 | a0001c0002t0001g0093 a0001c0002t0001g0116 |
2 | HG01106.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1778-259A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473870 | |||||||
| chr16:70473927 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1778-202C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473927 | |||||||
| chr16:70473938 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1778-191G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473938 | |||||||
| chr16:70473939 | G | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(13): Show |
24 | HG00738.hp2 HG01243.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1778-190G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473939 | |||||||
| chr16:70473955 | TGATCTCT others(1): Show |
T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1778-173_1778-166d others(10): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 15/23 | chr16 | 70473955 | |||||||
| chr16:70474446 | G | T | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1989-82G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 16/23 | chr16 | 70474446 | |||||||
| chr16:70474786 | A | G | 1 | a0001c0002t0001g0074 | 1 | NA18975.hp2 | splice_region_variant&intron_variant | LOW | c.2156-4A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 17/23 | chr16 | 70474786 | |||||||
| chr16:70475114 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2377+103G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 18/23 | chr16 | 70475114 | |||||||
| chr16:70475189 | A | G | 1 | a0004c0008t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2378-161A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 18/23 | chr16 | 70475189 | |||||||
| chr16:70475302 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2378-48G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 18/23 | chr16 | 70475302 | |||||||
| chr16:70475319 | G | A | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2378-31G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 18/23 | chr16 | 70475319 | |||||||
| chr16:70475523 | CGACT | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0152 a0001c0001t0001g0198 |
5 | NA18949.hp1 NA18950.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.2521+32_2521+35del others(4): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr16 | 70475523 | ||||||
| chr16:70475537 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2521+44C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 19/23 | chr16 | 70475537 | |||||||
| chr16:70475590 | G | A | 1 | a0001c0002t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2522-58G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 19/23 | chr16 | 70475590 | |||||||
| chr16:70475771 | T | G | 2 | a0001c0007t0001g0038 a0001c0007t0001g0039 |
2 | HG02723.hp1 HG03486.hp2 |
splice_region_variant&intron_variant | LOW | c.2641+4T>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70475771 | |||||||
| chr16:70475935 | A | C | 17 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(14): Show |
24 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2641+168A>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70475935 | |||||||
| chr16:70475964 | C | T | 18 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(15): Show |
31 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.2641+197C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70475964 | |||||||
| chr16:70475985 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0004g0170 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2641+218G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70475985 | |||||||
| chr16:70476010 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2641+243T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476010 | |||||||
| chr16:70476042 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2641+275G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476042 | |||||||
| chr16:70476066 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2641+299G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476066 | |||||||
| chr16:70476081 | C | G | 1 | a0001c0002t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2641+314C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476081 | |||||||
| chr16:70476096 | G | A | 5 | a0002c0004t0002g0004 a0002c0004t0002g0046 a0002c0004t0002g0047 others(2): Show |
12 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2641+329G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476096 | |||||||
| chr16:70476150 | CTG | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2641+384_2641+385d others(4): Show |
FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476150 | |||||||
| chr16:70476151 | T | C | 4 | a0001c0002t0001g0016 a0001c0002t0001g0018 a0001c0002t0001g0064 others(1): Show |
7 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641+384T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476151 | |||||||
| chr16:70476254 | C | T | 17 | a0001c0002t0001g0013 a0001c0002t0001g0030 a0001c0002t0001g0059 others(14): Show |
21 | HG00642.hp1 HG00735.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.2641+487C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476254 | |||||||
| chr16:70476292 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2641+525C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476292 | |||||||
| chr16:70476388 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2641+621C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476388 | |||||||
| chr16:70476398 | T | C | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641+631T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476398 | |||||||
| chr16:70476467 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2641+700C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476467 | |||||||
| chr16:70476534 | C | G | 4 | a0001c0007t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641+767C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476534 | |||||||
| chr16:70476638 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(10): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2641+871C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476638 | |||||||
| chr16:70476768 | A | G | 1 | a0001c0002t0001g0089 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2641+1001A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70476768 | |||||||
| chr16:70477149 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2642-1123C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477149 | |||||||
| chr16:70477241 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2642-1031G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477241 | |||||||
| chr16:70477273 | C | T | 2 | a0001c0001t0001g0035 a0001c0020t0001g0035 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2642-999C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477273 | |||||||
| chr16:70477326 | G | A | 2 | a0001c0007t0001g0038 a0001c0007t0001g0039 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2642-946G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477326 | |||||||
| chr16:70477386 | G | A | 1 | a0005c0011t0001g0026 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2642-886G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477386 | |||||||
| chr16:70477477 | C | T | 17 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(14): Show |
30 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.2642-795C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477477 | |||||||
| chr16:70477623 | C | T | 2 | a0001c0002t0001g0087 a0001c0002t0001g0097 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2642-649C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477623 | |||||||
| chr16:70477675 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0123 others(18): Show |
36 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.2642-597A>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70477675 | |||||||
| chr16:70478032 | T | C | 1 | a0001c0002t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2642-240T>C | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70478032 | |||||||
| chr16:70478180 | G | T | 4 | a0004c0008t0001g0027 a0004c0008t0001g0049 a0004c0008t0001g0051 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2642-92G>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70478180 | |||||||
| chr16:70478190 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2642-82G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70478190 | |||||||
| chr16:70478240 | G | A | 12 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(9): Show |
18 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2642-32G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70478240 | |||||||
| chr16:70478243 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2642-29T>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 20/23 | chr16 | 70478243 | |||||||
| chr16:70478502 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0142 a0001c0001t0001g0158 others(1): Show |
5 | HG01261.hp2 HG02148.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.2829+43G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 21/23 | chr16 | 70478502 | |||||||
| chr16:70478539 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2830-12C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 21/23 | chr16 | 70478539 | |||||||
| chr16:70478920 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2930-260C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70478920 | |||||||
| chr16:70479053 | C | T | 8 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(5): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2930-127C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70479053 | |||||||
| chr16:70479066 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0166 |
2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2930-114C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70479066 | |||||||
| chr16:70479072 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2930-108C>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70479072 | |||||||
| chr16:70479107 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0127 |
3 | HG01255.hp1 NA18952.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2930-73C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70479107 | |||||||
| chr16:70479112 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2930-68C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 22/23 | chr16 | 70479112 | |||||||
| chr16:70479407 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0176 |
2 | HG02257.hp1 HG02717.hp1 |
splice_region_variant&intron_variant | LOW | c.3153+4C>T | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 23/23 | chr16 | 70479407 | |||||||
| chr16:70479469 | G | A | 12 | a0001c0003t0001g0011 a0001c0003t0001g0045 a0001c0003t0001g0053 others(9): Show |
18 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3153+66G>A | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 23/23 | chr16 | 70479469 | |||||||
| chr16:70479481 | C | G | 60 | a0001c0001t0001g0115 a0001c0001t0001g0183 a0001c0001t0001g0186 others(57): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.3153+78C>G | FCSK | ENSG00000157353.17 | transcript | ENST00000288078.11 | protein_coding | 23/23 | chr16 | 70479481 |