Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9457 |
| ensemblid | ENSG00000112214.11 |
| hgncid | 17371 |
| symbol | FHL5 |
| name | four and a half LIM domains 5 |
| refseq_nuc | NM_001322466.2 |
| refseq_prot | NP_001309395.1 |
| ensembl_nuc | ENST00000450218.6 |
| ensembl_prot | ENSP00000396390.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 96563128 |
| end | 96618626 |
| strand | + |
| ver | v1.2 |
| region | chr6:96563128-96618626 |
| region5000 | chr6:96558128-96623626 |
| regionname0 | FHL5_chr6_96563128_96618626 |
| regionname5000 | FHL5_chr6_96558128_96623626 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 284 | 198 | 48 | 25 | 94 | 7 | 23 | 80 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0002 | 0/0 | 284 | 97 | 3 | 27 | 53 | 4 | 10 | 39 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0003 | 1/0 | 284 | 71 | 26 | 16 | 14 | 3 | 11 | 14 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0004 | 0/0 | 284 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0005 | 0/0 | 284 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0006 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| a0007 | 0/0 | 284 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | MTTAH others(279): Show |
chr6 | 96558128 | 96623626 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 852 | 141 | 38 | 12 | 73 | 2 | 15 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0001c0004 | 0/0 | 852 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0001c0007 | 0/0 | 852 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0001c0012 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0002c0002 | 0/0 | 852 | 97 | 3 | 27 | 53 | 4 | 10 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0003c0003 | 1/0 | 852 | 71 | 26 | 16 | 14 | 3 | 11 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0004c0005 | 0/0 | 852 | 5 | 5 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0004c0010 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0004c0013 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0005c0006 | 0/0 | 852 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0005c0008 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0006c0009 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 | ||
| a0007c0011 | 0/0 | 852 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | ATGAC others(847): Show |
chr6 | 96558128 | 96623626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 3947 | 82 | 6 | 6 | 60 | 0 | 9 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0004 | 0/0 | 3947 | 42 | 22 | 1 | 13 | 0 | 6 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0007 | 0/0 | 3947 | 6 | 1 | 3 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0009 | 0/0 | 3947 | 5 | 4 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0012 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0013 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0014 | 0/0 | 3949 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0016 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0019 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0001t0021 | 0/0 | 3947 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0004t0003 | 0/0 | 3947 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0007t0004 | 0/0 | 3947 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0001c0012t0020 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0001 | 0/0 | 3949 | 83 | 2 | 18 | 53 | 3 | 7 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0004 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0005 | 0/0 | 3947 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0006 | 0/0 | 3949 | 7 | 0 | 7 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0011 | 0/0 | 3949 | 3 | 0 | 2 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0002c0002t0015 | 0/0 | 3949 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0001 | 1/0 | 3949 | 49 | 18 | 8 | 11 | 2 | 9 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0004 | 0/0 | 3947 | 6 | 5 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0005 | 0/0 | 3947 | 7 | 0 | 5 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0008 | 0/0 | 3949 | 5 | 0 | 2 | 0 | 1 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0010 | 0/0 | 3949 | 3 | 3 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0003c0003t0017 | 0/0 | 3949 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0004c0005t0001 | 0/0 | 3949 | 3 | 3 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0004c0005t0004 | 0/0 | 3947 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0004c0010t0022 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0004c0013t0018 | 0/0 | 3949 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| a0005c0006t0004 | 0/0 | 3947 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0005c0008t0012 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0006c0009t0004 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3942): Show |
chr6 | 96558128 | 96623626 |
| a0007c0011t0001 | 0/0 | 3949 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | AGTAG others(3944): Show |
chr6 | 96558128 | 96623626 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0007g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0016g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0001t0021g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0004t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0007t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0001c0012t0020g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0001 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0011g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0002c0002t0015g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0004 | 1/0 | 6 | 0 | 1 | 0 | 1 | 3 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0004g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0008g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0008g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0003c0003t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0005t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0010t0022g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0004c0013t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0005c0006t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0005c0006t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0005c0008t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0006c0009t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| a0007c0011t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0011 | g0001 | EUR | GBR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0004 | EUR | GBR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0033 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00280 | hp2 | a0001 | c0004 | t0003 | g0011 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00323 | hp1 | a0001 | c0004 | t0003 | g0011 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0106 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00642 | hp1 | a0003 | c0003 | t0005 | g0123 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00642 | hp2 | a0002 | c0002 | t0006 | g0163 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0064 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00741 | hp1 | a0001 | c0004 | t0003 | g0051 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0280 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01069 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01070 | hp1 | a0003 | c0003 | t0005 | g0120 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0056 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01071 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01074 | hp1 | a0002 | c0002 | t0011 | g0147 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01074 | hp2 | a0001 | c0004 | t0003 | g0248 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01081 | hp1 | a0001 | c0004 | t0003 | g0045 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0019 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01167 | hp1 | a0002 | c0002 | t0006 | g0164 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01167 | hp2 | a0003 | c0003 | t0005 | g0127 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01168 | hp1 | a0002 | c0002 | t0011 | g0148 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01169 | hp1 | a0002 | c0002 | t0006 | g0165 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0261 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01192 | hp2 | a0002 | c0002 | t0006 | g0015 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0046 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01256 | hp2 | a0001 | c0004 | t0003 | g0045 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01257 | hp2 | a0003 | c0003 | t0008 | g0028 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01258 | hp2 | a0003 | c0003 | t0008 | g0028 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01358 | hp1 | a0003 | c0003 | t0005 | g0013 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01358 | hp2 | a0001 | c0004 | t0003 | g0046 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01433 | hp2 | a0001 | c0004 | t0003 | g0044 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01496 | hp2 | a0003 | c0003 | t0004 | g0037 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01515 | hp1 | a0001 | c0004 | t0003 | g0260 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0054 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01516 | hp2 | a0003 | c0003 | t0008 | g0136 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0019 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01517 | hp2 | a0001 | c0004 | t0003 | g0259 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01952 | hp1 | a0001 | c0004 | t0003 | g0249 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0118 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01981 | hp2 | a0002 | c0002 | t0006 | g0015 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02004 | hp1 | a0002 | c0002 | t0006 | g0039 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0177 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0170 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CDX | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CDX | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02257 | hp1 | a0005 | c0008 | t0012 | g0068 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0048 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02258 | hp1 | a0003 | c0003 | t0004 | g0230 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02293 | hp1 | a0001 | c0001 | t0021 | g0074 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0032 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02300 | hp1 | a0001 | c0004 | t0003 | g0005 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02300 | hp2 | a0002 | c0002 | t0006 | g0168 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02602 | hp1 | a0001 | c0004 | t0003 | g0005 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02622 | hp1 | a0003 | c0003 | t0004 | g0174 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02630 | hp1 | a0004 | c0005 | t0001 | g0069 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02698 | hp2 | a0001 | c0004 | t0003 | g0254 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0279 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02723 | hp2 | a0004 | c0005 | t0001 | g0067 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02735 | hp2 | a0003 | c0003 | t0008 | g0128 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02738 | hp1 | a0001 | c0004 | t0003 | g0268 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0265 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02809 | hp2 | a0003 | c0003 | t0010 | g0203 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02895 | hp1 | a0004 | c0005 | t0004 | g0041 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02895 | hp2 | a0003 | c0003 | t0010 | g0202 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0142 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02897 | hp2 | a0004 | c0005 | t0004 | g0041 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0144 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0206 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0263 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0175 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03017 | hp2 | a0001 | c0004 | t0003 | g0255 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03041 | hp2 | a0005 | c0006 | t0004 | g0244 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03130 | hp1 | a0004 | c0013 | t0018 | g0052 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0274 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0047 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0278 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03453 | hp1 | a0004 | c0010 | t0022 | g0059 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0125 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03491 | hp2 | a0002 | c0002 | t0005 | g0193 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0072 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0176 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03579 | hp2 | a0005 | c0006 | t0004 | g0243 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03669 | hp1 | a0003 | c0003 | t0008 | g0135 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03704 | hp2 | a0002 | c0002 | t0015 | g0158 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0013 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03831 | hp2 | a0002 | c0002 | t0005 | g0035 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0126 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03942 | hp1 | a0001 | c0004 | t0003 | g0258 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0129 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04115 | hp1 | a0001 | c0004 | t0003 | g0251 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04184 | hp2 | a0001 | c0004 | t0003 | g0266 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0121 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0130 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04204 | hp2 | a0001 | c0004 | t0003 | g0044 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18522 | hp1 | a0003 | c0003 | t0004 | g0179 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18522 | hp2 | a0006 | c0009 | t0004 | g0238 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0237 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18906 | hp2 | a0001 | c0004 | t0003 | g0252 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18944 | hp1 | a0001 | c0004 | t0003 | g0271 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18950 | hp1 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18952 | hp1 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18957 | hp2 | a0001 | c0004 | t0003 | g0273 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18959 | hp1 | a0001 | c0004 | t0003 | g0272 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18964 | hp1 | a0001 | c0004 | t0003 | g0269 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18967 | hp1 | a0001 | c0004 | t0003 | g0262 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18968 | hp2 | a0003 | c0003 | t0017 | g0173 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18969 | hp1 | a0003 | c0003 | t0005 | g0032 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18972 | hp1 | a0001 | c0004 | t0003 | g0245 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18973 | hp1 | a0001 | c0004 | t0003 | g0049 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18975 | hp1 | a0001 | c0004 | t0003 | g0253 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18979 | hp2 | a0001 | c0004 | t0003 | g0057 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18981 | hp2 | a0001 | c0004 | t0003 | g0257 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18986 | hp2 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18989 | hp2 | a0003 | c0003 | t0005 | g0195 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18998 | hp1 | a0001 | c0004 | t0003 | g0256 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19002 | hp1 | a0007 | c0011 | t0001 | g0154 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19002 | hp2 | a0001 | c0004 | t0003 | g0049 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0119 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0267 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19043 | hp2 | a0003 | c0003 | t0004 | g0037 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19058 | hp1 | a0001 | c0004 | t0003 | g0250 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19072 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19075 | hp1 | a0001 | c0007 | t0004 | g0214 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19076 | hp1 | a0001 | c0004 | t0003 | g0264 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19078 | hp2 | a0001 | c0004 | t0003 | g0246 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19085 | hp1 | a0001 | c0004 | t0003 | g0270 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19088 | hp2 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0071 | AFR | ASW | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0063 | AFR | ASW | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20752 | hp1 | a0001 | c0004 | t0003 | g0050 | EUR | TSI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0039 | EUR | TSI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01123 | hp1 | a0001 | c0004 | t0003 | g0247 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG01123 | hp2 | a0003 | c0003 | t0005 | g0122 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02109 | hp2 | a0004 | c0005 | t0001 | g0065 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02486 | hp1 | a0001 | c0004 | t0003 | g0047 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG02559 | hp2 | a0001 | c0004 | t0003 | g0048 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03471 | hp1 | a0003 | c0003 | t0010 | g0201 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0178 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0281 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20300 | hp1 | a0003 | c0003 | t0004 | g0200 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0277 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| NA21309 | hp2 | a0001 | c0012 | t0020 | g0116 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0109 | REF | REF | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0004 | REF | REF | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96610671 | A | C | 1 | a0007 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.604A>C | p.Met202Leu | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 844/3949 | 604/855 | 202/284 | chr6 | 96610671 | |||
| chr6:96610677 | A | G | 3 | a0001 a0004 a0006 |
205 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
missense_variant | MODERATE | c.610A>G | p.Arg204Gly | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 850/3949 | 610/855 | 204/284 | chr6 | 96610677 | |||
| chr6:96610698 | G | A | 2 | a0002 a0007 |
98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
missense_variant | MODERATE | c.631G>A | p.Val211Met | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 871/3949 | 631/855 | 211/284 | chr6 | 96610698 | |||
| chr6:96610741 | G | T | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.674G>T | p.Cys225Phe | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 914/3949 | 674/855 | 225/284 | chr6 | 96610741 | |||
| chr6:96615646 | C | G | 3 | a0001 a0005 a0006 |
201 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(198): Show |
missense_variant | MODERATE | c.729C>G | p.Ser243Arg | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 969/3949 | 729/855 | 243/284 | chr6 | 96615646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96604821 | G | C | 1 | a0005c0006 | 2 | HG03041.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.231G>C | p.Val77Val | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/6 | 471/3949 | 231/855 | 77/284 | chr6 | 96604821 | |||
| chr6:96604878 | C | T | 3 | a0001c0004 a0001c0012 a0004c0013 |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
synonymous_variant | LOW | c.288C>T | p.Asn96Asn | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/6 | 528/3949 | 288/855 | 96/284 | chr6 | 96604878 | |||
| chr6:96610601 | T | C | 1 | a0001c0007 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.534T>C | p.Cys178Cys | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 774/3949 | 534/855 | 178/284 | chr6 | 96610601 | |||
| chr6:96610691 | A | G | 3 | a0001c0004 a0004c0010 a0004c0013 |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
synonymous_variant | LOW | c.624A>G | p.Pro208Pro | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 864/3949 | 624/855 | 208/284 | chr6 | 96610691 | |||
| chr6:96615679 | A | G | 8 | a0001c0001 a0001c0004 a0001c0007 others(5): Show |
202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
synonymous_variant | LOW | c.762A>G | p.Lys254Lys | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1002/3949 | 762/855 | 254/284 | chr6 | 96615679 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96615848 | T | G | 1 | a0001c0001t0002 | 81 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*76T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 76 | chr6 | 96615848 | ||||||
| chr6:96615960 | A | G | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 188 | chr6 | 96615960 | ||||||
| chr6:96615987 | T | C | 4 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0014 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*215T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 215 | chr6 | 96615987 | ||||||
| chr6:96616044 | C | G | 1 | a0001c0001t0021 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 272 | chr6 | 96616044 | ||||||
| chr6:96616108 | T | C | 1 | a0002c0002t0015 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 336 | chr6 | 96616108 | ||||||
| chr6:96616146 | G | A | 1 | a0001c0001t0013 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 374 | chr6 | 96616146 | ||||||
| chr6:96616350 | T | C | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 578 | chr6 | 96616350 | ||||||
| chr6:96616603 | G | A | 1 | a0002c0002t0006 | 7 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*831G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 831 | chr6 | 96616603 | ||||||
| chr6:96616929 | CCA | C | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(18): Show |
219 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1161_*1162delAC | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1161 | INFO_REALIGN_3_PRIME | chr6 | 96616929 | |||||
| chr6:96616937 | C | A | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(18): Show |
219 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1165C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1165 | chr6 | 96616937 | ||||||
| chr6:96617255 | C | T | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
210 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1483 | chr6 | 96617255 | ||||||
| chr6:96617263 | T | C | 1 | a0001c0001t0007 | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1491T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1491 | chr6 | 96617263 | ||||||
| chr6:96617336 | G | A | 2 | a0001c0001t0007 a0001c0004t0003 |
61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1564G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1564 | chr6 | 96617336 | ||||||
| chr6:96617392 | A | C | 1 | a0003c0003t0017 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1620A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1620 | chr6 | 96617392 | ||||||
| chr6:96617460 | G | A | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1688 | chr6 | 96617460 | ||||||
| chr6:96617627 | T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1855 | chr6 | 96617627 | ||||||
| chr6:96617727 | T | C | 1 | a0003c0003t0010 | 3 | HG02809.hp2 HG02895.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1955 | chr6 | 96617727 | ||||||
| chr6:96617785 | A | G | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
210 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2013A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2013 | chr6 | 96617785 | ||||||
| chr6:96617807 | C | T | 1 | a0001c0012t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2035 | chr6 | 96617807 | ||||||
| chr6:96617818 | G | C | 1 | a0002c0002t0011 | 3 | HG00140.hp1 HG01074.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2046G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2046 | chr6 | 96617818 | ||||||
| chr6:96617875 | G | A | 2 | a0001c0001t0007 a0001c0004t0003 |
61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2103G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2103 | chr6 | 96617875 | ||||||
| chr6:96617985 | G | A | 2 | a0001c0001t0002 a0003c0003t0008 |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2213G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2213 | chr6 | 96617985 | ||||||
| chr6:96617989 | G | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2217G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2217 | chr6 | 96617989 | ||||||
| chr6:96618033 | G | C | 1 | a0001c0001t0009 | 5 | HG00733.hp2 HG02572.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2261G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2261 | chr6 | 96618033 | ||||||
| chr6:96618056 | C | T | 1 | a0001c0001t0019 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2284C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2284 | chr6 | 96618056 | ||||||
| chr6:96618144 | C | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2372 | chr6 | 96618144 | ||||||
| chr6:96618160 | T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2388T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2388 | chr6 | 96618160 | ||||||
| chr6:96618322 | A | T | 1 | a0002c0002t0015 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2550 | chr6 | 96618322 | ||||||
| chr6:96618366 | C | T | 1 | a0001c0004t0003 | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2594C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2594 | chr6 | 96618366 | ||||||
| chr6:96618406 | T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2634T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2634 | chr6 | 96618406 | ||||||
| chr6:96618447 | C | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2675C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2675 | chr6 | 96618447 | ||||||
| chr6:96618453 | C | G | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
210 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2681C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2681 | chr6 | 96618453 | ||||||
| chr6:96618479 | A | T | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
210 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2707A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2707 | chr6 | 96618479 | ||||||
| chr6:96618506 | T | C | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
210 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2734T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2734 | chr6 | 96618506 | ||||||
| chr6:96618561 | C | T | 1 | a0004c0013t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2789C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2789 | chr6 | 96618561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96563383 | T | A | 2 | a0001c0004t0003g0050 a0001c0004t0003g0051 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-13+28T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96563383 | |||||||
| chr6:96563430 | T | A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+75T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96563430 | |||||||
| chr6:96564216 | T | G | 1 | a0001c0004t0003g0057 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-13+861T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564216 | |||||||
| chr6:96564577 | CTG | C | 7 | a0003c0003t0001g0275 a0003c0003t0001g0276 a0003c0003t0001g0277 others(4): Show |
7 | HG00741.hp2 HG01884.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+1226_-13+1227d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96564577 | ||||||
| chr6:96564744 | G | C | 2 | a0001c0001t0009g0058 a0004c0010t0022g0059 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+1389G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564744 | |||||||
| chr6:96564870 | C | T | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+1515C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564870 | |||||||
| chr6:96564879 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0060 a0001c0001t0004g0061 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1524G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564879 | |||||||
| chr6:96564942 | A | T | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+1587A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564942 | |||||||
| chr6:96565048 | G | C | 1 | a0001c0001t0002g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+1693G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565048 | |||||||
| chr6:96565073 | A | G | 2 | a0001c0001t0009g0058 a0004c0010t0022g0059 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+1718A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565073 | |||||||
| chr6:96565094 | AAAAT | A | 43 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(40): Show |
50 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-13+1746_-13+1749d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96565094 | ||||||
| chr6:96565103 | A | T | 1 | a0001c0001t0004g0207 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-13+1748A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565103 | |||||||
| chr6:96565463 | A | G | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+2108A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565463 | |||||||
| chr6:96565486 | C | T | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+2131C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565486 | |||||||
| chr6:96565552 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-13+2197G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565552 | |||||||
| chr6:96565641 | A | G | 1 | a0003c0003t0001g0281 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-13+2286A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565641 | |||||||
| chr6:96565661 | G | T | 1 | a0002c0002t0001g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-13+2306G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565661 | |||||||
| chr6:96565750 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-13+2395C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565750 | |||||||
| chr6:96565938 | T | C | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(159): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-13+2583T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565938 | |||||||
| chr6:96566315 | C | T | 1 | a0001c0004t0003g0274 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13+2960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566315 | |||||||
| chr6:96566357 | C | T | 2 | a0001c0001t0009g0058 a0004c0010t0022g0059 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+3002C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566357 | |||||||
| chr6:96566379 | T | G | 40 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+3024T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566379 | |||||||
| chr6:96566530 | G | A | 2 | a0001c0001t0009g0058 a0004c0010t0022g0059 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+3175G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566530 | |||||||
| chr6:96566535 | A | G | 6 | a0001c0004t0003g0057 a0001c0004t0003g0269 a0001c0004t0003g0270 others(3): Show |
6 | NA18944.hp1 NA18957.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3180A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566535 | |||||||
| chr6:96566541 | C | T | 13 | a0001c0001t0004g0043 a0001c0001t0004g0228 a0001c0001t0004g0229 others(10): Show |
14 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+3186C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566541 | |||||||
| chr6:96566612 | T | C | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+3257T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566612 | |||||||
| chr6:96566649 | C | T | 1 | a0003c0003t0001g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-13+3294C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566649 | |||||||
| chr6:96566661 | T | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+3306T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566661 | |||||||
| chr6:96566720 | G | A | 2 | a0001c0001t0002g0070 a0002c0002t0001g0117 |
2 | HG00735.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-13+3365G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566720 | |||||||
| chr6:96566755 | T | A | 1 | a0001c0001t0009g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+3400T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566755 | |||||||
| chr6:96566971 | C | T | 277 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(274): Show |
362 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(359): Show |
intron_variant | MODIFIER | c.-13+3616C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566971 | |||||||
| chr6:96567071 | A | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+3716A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567071 | |||||||
| chr6:96567096 | G | T | 7 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(4): Show |
7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+3741G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567096 | |||||||
| chr6:96567429 | C | T | 10 | a0003c0003t0001g0275 a0003c0003t0001g0276 a0003c0003t0001g0277 others(7): Show |
10 | HG00741.hp2 HG01884.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+4074C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567429 | |||||||
| chr6:96567545 | C | T | 1 | a0003c0003t0004g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13+4190C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567545 | |||||||
| chr6:96567643 | T | C | 40 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+4288T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567643 | |||||||
| chr6:96567666 | T | A | 1 | a0002c0002t0001g0124 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-13+4311T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567666 | |||||||
| chr6:96567694 | A | G | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-13+4339A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567694 | |||||||
| chr6:96567731 | CT | C | 40 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+4383delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567731 | ||||||
| chr6:96567769 | AT | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-13+4422delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567769 | ||||||
| chr6:96567825 | C | CT | 55 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(52): Show |
80 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-13+4487dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | ||||||
| chr6:96567825 | C | CTT | 10 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0112 others(7): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13+4486_-13+4487d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | ||||||
| chr6:96567825 | C | CTTTT | 65 | a0001c0001t0004g0018 a0001c0001t0004g0042 a0001c0001t0004g0043 others(62): Show |
83 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-13+4484_-13+4487d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | ||||||
| chr6:96567825 | C | CTTTTT | 9 | a0001c0001t0004g0020 a0001c0001t0004g0061 a0001c0001t0004g0227 others(6): Show |
10 | HG02280.hp1 HG02738.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+4483_-13+4487d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | ||||||
| chr6:96567825 | CT | C | 18 | a0001c0001t0002g0040 a0001c0001t0009g0058 a0001c0001t0012g0072 others(15): Show |
20 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+4487delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | ||||||
| chr6:96568423 | T | C | 6 | a0001c0004t0003g0044 a0001c0004t0003g0045 a0001c0004t0003g0046 others(3): Show |
9 | HG01074.hp2 HG01081.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+5068T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568423 | |||||||
| chr6:96568634 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13+5279G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568634 | |||||||
| chr6:96568729 | G | A | 1 | a0001c0001t0004g0229 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13+5374G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568729 | |||||||
| chr6:96568804 | G | A | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+5449G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568804 | |||||||
| chr6:96568845 | C | T | 40 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+5490C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568845 | |||||||
| chr6:96568889 | A | G | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13+5534A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568889 | |||||||
| chr6:96568925 | T | C | 1 | a0003c0003t0004g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-13+5570T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568925 | |||||||
| chr6:96568976 | C | T | 2 | a0003c0003t0005g0122 a0003c0003t0005g0123 |
2 | HG00642.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-13+5621C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568976 | |||||||
| chr6:96568993 | T | G | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+5638T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568993 | |||||||
| chr6:96569305 | T | C | 1 | a0003c0003t0001g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-13+5950T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569305 | |||||||
| chr6:96569449 | T | C | 1 | a0001c0001t0019g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13+6094T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569449 | |||||||
| chr6:96569650 | G | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+6295G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569650 | |||||||
| chr6:96569794 | A | AGTGAGTT others(314): Show |
1 | a0001c0004t0003g0250 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-13+6452_-13+6453i others(323): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | ||||||
| chr6:96569794 | A | AGTGAGTT others(315): Show |
35 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-13+6452_-13+6453i others(324): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | ||||||
| chr6:96569794 | A | AGTGAGTT others(315): Show |
1 | a0001c0004t0003g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-13+6452_-13+6453i others(324): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | ||||||
| chr6:96569794 | A | AGTGAGTT others(316): Show |
4 | a0001c0004t0003g0049 a0001c0004t0003g0057 a0001c0004t0003g0265 others(1): Show |
5 | HG02738.hp1 HG02809.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+6452_-13+6453i others(325): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | ||||||
| chr6:96569824 | G | T | 1 | a0001c0001t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+6469G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569824 | |||||||
| chr6:96569825 | G | T | 1 | a0001c0001t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+6470G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569825 | |||||||
| chr6:96569827 | CT | C | 39 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0042 others(36): Show |
44 | HG00408.hp1 HG00544.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.-13+6484delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569827 | ||||||
| chr6:96569855 | T | C | 3 | a0001c0001t0004g0017 a0001c0001t0004g0210 a0001c0001t0004g0211 |
5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+6500T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569855 | |||||||
| chr6:96570315 | C | T | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+6960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570315 | |||||||
| chr6:96570528 | C | G | 6 | a0002c0002t0001g0039 a0002c0002t0001g0117 a0002c0002t0001g0192 others(3): Show |
6 | HG00735.hp2 HG01106.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+7173C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570528 | |||||||
| chr6:96570944 | T | C | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+7589T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570944 | |||||||
| chr6:96571301 | G | A | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG01952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-13+7946G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571301 | |||||||
| chr6:96571313 | G | A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+7958G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571313 | |||||||
| chr6:96571595 | G | T | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+8240G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571595 | |||||||
| chr6:96571599 | C | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+8244C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571599 | |||||||
| chr6:96571766 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-13+8411C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571766 | |||||||
| chr6:96571872 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-13+8517A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571872 | |||||||
| chr6:96571912 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-13+8557C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571912 | |||||||
| chr6:96571962 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-13+8607G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571962 | |||||||
| chr6:96572214 | G | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8859G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572214 | |||||||
| chr6:96572244 | G | T | 3 | a0002c0002t0001g0038 a0002c0002t0001g0188 a0002c0002t0001g0189 |
4 | HG01081.hp2 HG01255.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8889G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572244 | |||||||
| chr6:96572422 | A | G | 2 | a0003c0003t0001g0106 a0003c0003t0001g0107 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-13+9067A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572422 | |||||||
| chr6:96572601 | T | C | 1 | a0002c0002t0004g0142 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-13+9246T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572601 | |||||||
| chr6:96572710 | G | T | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+9355G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572710 | |||||||
| chr6:96572732 | T | C | 1 | a0001c0001t0004g0213 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+9377T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572732 | |||||||
| chr6:96572778 | C | G | 1 | a0001c0001t0002g0105 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-13+9423C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572778 | |||||||
| chr6:96572845 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-13+9490A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572845 | |||||||
| chr6:96572978 | C | T | 3 | a0003c0003t0008g0028 a0003c0003t0008g0135 a0003c0003t0008g0136 |
4 | HG01257.hp2 HG01258.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+9623C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572978 | |||||||
| chr6:96573028 | AAAG | A | 37 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0042 others(34): Show |
42 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13+9678_-13+9680d others(5): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573028 | ||||||
| chr6:96573041 | C | A | 58 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(55): Show |
73 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-13+9686C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573041 | |||||||
| chr6:96573146 | G | A | 2 | a0001c0004t0003g0251 a0001c0004t0003g0266 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-13+9791G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573146 | |||||||
| chr6:96573217 | T | G | 9 | a0003c0003t0001g0125 a0003c0003t0001g0126 a0003c0003t0001g0129 others(6): Show |
10 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+9862T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573217 | |||||||
| chr6:96573527 | A | AT | 44 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(41): Show |
49 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-13+10196dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | ||||||
| chr6:96573527 | A | ATT | 10 | a0001c0001t0004g0043 a0001c0001t0004g0228 a0001c0001t0004g0233 others(7): Show |
11 | HG01106.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10195_-13+1019 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | ||||||
| chr6:96573527 | AT | A | 18 | a0001c0001t0002g0062 a0001c0001t0002g0075 a0001c0001t0002g0076 others(15): Show |
20 | HG01109.hp2 HG01981.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+10196delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | ||||||
| chr6:96573527 | ATT | A | 9 | a0001c0001t0004g0213 a0001c0001t0007g0019 a0001c0001t0007g0053 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+10195_-13+1019 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | ||||||
| chr6:96573577 | A | G | 1 | a0003c0003t0004g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-13+10222A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573577 | |||||||
| chr6:96573582 | C | T | 44 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(41): Show |
51 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-13+10227C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573582 | |||||||
| chr6:96573593 | C | T | 3 | a0001c0004t0003g0045 a0001c0004t0003g0046 a0001c0004t0003g0249 |
5 | HG01081.hp1 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+10238C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573593 | |||||||
| chr6:96573615 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+10260G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573615 | |||||||
| chr6:96573635 | C | A | 44 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(41): Show |
51 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-13+10280C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573635 | |||||||
| chr6:96573743 | G | A | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+10388G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573743 | |||||||
| chr6:96573749 | C | G | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+10394C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573749 | |||||||
| chr6:96573811 | G | A | 2 | a0001c0001t0002g0077 a0002c0002t0001g0124 |
2 | HG00673.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-13+10456G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573811 | |||||||
| chr6:96573839 | G | T | 4 | a0001c0004t0003g0048 a0001c0004t0003g0261 a0001c0004t0003g0263 others(1): Show |
5 | HG01192.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+10484G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573839 | |||||||
| chr6:96574083 | A | G | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+10728A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574083 | |||||||
| chr6:96574141 | G | A | 1 | a0002c0002t0001g0145 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-13+10786G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574141 | |||||||
| chr6:96574164 | G | T | 7 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(4): Show |
7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+10809G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574164 | |||||||
| chr6:96574592 | C | T | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(159): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-13+11237C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574592 | |||||||
| chr6:96574776 | T | A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+11421T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574776 | |||||||
| chr6:96574838 | T | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+11483T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574838 | |||||||
| chr6:96574853 | C | G | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+11498C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574853 | |||||||
| chr6:96574939 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+11584A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574939 | |||||||
| chr6:96575062 | C | G | 185 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(182): Show |
236 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-13+11707C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575062 | |||||||
| chr6:96575150 | G | A | 185 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(182): Show |
236 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-13+11795G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575150 | |||||||
| chr6:96575194 | G | A | 93 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(90): Show |
122 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-13+11839G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575194 | |||||||
| chr6:96575232 | C | A | 1 | a0003c0003t0001g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-13+11877C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575232 | |||||||
| chr6:96575383 | T | G | 1 | a0003c0003t0001g0146 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-13+12028T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575383 | |||||||
| chr6:96575385 | C | T | 21 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(18): Show |
25 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13+12030C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575385 | |||||||
| chr6:96575403 | C | T | 5 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 others(2): Show |
5 | HG00544.hp2 NA18970.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+12048C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575403 | |||||||
| chr6:96575565 | C | T | 1 | a0001c0001t0004g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-13+12210C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575565 | |||||||
| chr6:96575568 | A | G | 9 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(6): Show |
9 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+12213A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575568 | |||||||
| chr6:96575589 | G | A | 2 | a0002c0002t0011g0147 a0002c0002t0011g0148 |
2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-13+12234G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575589 | |||||||
| chr6:96575590 | G | T | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+12235G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575590 | |||||||
| chr6:96575656 | G | T | 1 | a0002c0002t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-13+12301G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575656 | |||||||
| chr6:96575756 | T | C | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+12401T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575756 | |||||||
| chr6:96575795 | G | A | 4 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0225 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+12440G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575795 | |||||||
| chr6:96575908 | T | C | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+12553T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575908 | |||||||
| chr6:96575911 | G | T | 1 | a0001c0001t0004g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-13+12556G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575911 | |||||||
| chr6:96576030 | C | G | 1 | a0001c0004t0003g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+12675C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576030 | |||||||
| chr6:96576063 | A | G | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+12708A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576063 | |||||||
| chr6:96576073 | C | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+12718C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576073 | |||||||
| chr6:96576289 | G | A | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-13+12934G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576289 | |||||||
| chr6:96576460 | C | T | 1 | a0003c0003t0001g0199 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-13+13105C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576460 | |||||||
| chr6:96576527 | C | A | 1 | a0005c0006t0004g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-13+13172C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576527 | |||||||
| chr6:96576812 | A | G | 2 | a0001c0004t0003g0011 a0001c0004t0003g0268 |
5 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+13457A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576812 | |||||||
| chr6:96576941 | C | T | 1 | a0003c0003t0017g0173 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-13+13586C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576941 | |||||||
| chr6:96577368 | C | T | 11 | a0001c0001t0004g0043 a0001c0001t0004g0228 a0001c0001t0004g0229 others(8): Show |
12 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+14013C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577368 | |||||||
| chr6:96577588 | T | A | 1 | a0001c0001t0004g0217 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-13+14233T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577588 | |||||||
| chr6:96577620 | C | T | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+14265C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577620 | |||||||
| chr6:96577868 | A | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0086 a0001c0001t0002g0108 |
4 | NA18948.hp2 NA18962.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+14513A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577868 | |||||||
| chr6:96577941 | C | CA | 6 | a0001c0004t0003g0253 a0001c0004t0003g0262 a0003c0003t0001g0106 others(3): Show |
6 | HG00323.hp2 HG01106.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+14603dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96577941 | ||||||
| chr6:96577941 | CA | C | 8 | a0001c0001t0002g0108 a0001c0001t0004g0061 a0001c0001t0004g0236 others(5): Show |
9 | HG00280.hp1 HG01070.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+14603delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96577941 | ||||||
| chr6:96577945 | A | C | 1 | a0002c0002t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-13+14590A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577945 | |||||||
| chr6:96578109 | T | C | 9 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(6): Show |
9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+14754T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578109 | |||||||
| chr6:96578313 | T | A | 1 | a0001c0001t0002g0087 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-13+14958T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578313 | |||||||
| chr6:96578408 | G | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+15053G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578408 | |||||||
| chr6:96578553 | G | A | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+15198G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578553 | |||||||
| chr6:96578580 | G | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+15225G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578580 | |||||||
| chr6:96578714 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+15359C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578714 | |||||||
| chr6:96578736 | G | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+15381G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578736 | |||||||
| chr6:96578906 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-13+15551T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578906 | |||||||
| chr6:96579086 | C | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+15731C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579086 | |||||||
| chr6:96579154 | T | A | 1 | a0001c0001t0002g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-13+15799T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579154 | |||||||
| chr6:96579504 | C | T | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(159): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-13+16149C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579504 | |||||||
| chr6:96579643 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+16288C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579643 | |||||||
| chr6:96579829 | GA | G | 40 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+16475delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579829 | |||||||
| chr6:96579983 | C | G | 1 | a0003c0003t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13+16628C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579983 | |||||||
| chr6:96580016 | A | G | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+16661A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580016 | |||||||
| chr6:96580066 | C | T | 43 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13+16711C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580066 | |||||||
| chr6:96580067 | G | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+16712G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580067 | |||||||
| chr6:96580311 | G | T | 1 | a0003c0003t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+16956G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580311 | |||||||
| chr6:96580499 | G | T | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+17144G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580499 | |||||||
| chr6:96580551 | C | T | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+17196C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580551 | |||||||
| chr6:96580581 | C | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+17226C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580581 | |||||||
| chr6:96580733 | T | A | 1 | a0001c0001t0004g0213 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+17378T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580733 | |||||||
| chr6:96581203 | T | C | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+17848T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581203 | |||||||
| chr6:96581389 | A | G | 37 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0042 others(34): Show |
42 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13+18034A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581389 | |||||||
| chr6:96581429 | G | A | 52 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(49): Show |
77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-13+18074G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581429 | |||||||
| chr6:96581469 | T | C | 3 | a0001c0001t0012g0072 a0001c0001t0013g0073 a0001c0001t0014g0071 |
3 | HG02886.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+18114T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581469 | |||||||
| chr6:96581590 | G | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+18235G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581590 | |||||||
| chr6:96581995 | G | A | 91 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(88): Show |
114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-13+18640G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581995 | |||||||
| chr6:96582078 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-13+18723T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582078 | |||||||
| chr6:96582114 | G | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+18759G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582114 | |||||||
| chr6:96582315 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+18960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582315 | |||||||
| chr6:96582332 | A | T | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18977A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582332 | |||||||
| chr6:96582730 | C | T | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+19375C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582730 | |||||||
| chr6:96582735 | A | G | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+19380A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582735 | |||||||
| chr6:96582837 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0113 |
3 | HG02738.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-13+19482G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582837 | |||||||
| chr6:96582866 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-13+19511C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582866 | |||||||
| chr6:96583093 | C | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19738C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583093 | |||||||
| chr6:96583211 | C | T | 10 | a0003c0003t0001g0006 a0003c0003t0001g0007 a0003c0003t0001g0032 others(7): Show |
18 | HG01099.hp2 HG01978.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+19856C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583211 | |||||||
| chr6:96583250 | C | T | 8 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(5): Show |
8 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+19895C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583250 | |||||||
| chr6:96583329 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13+19974T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583329 | |||||||
| chr6:96583613 | G | A | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-19989G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583613 | |||||||
| chr6:96583627 | A | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0060 a0001c0001t0004g0061 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-19975A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583627 | |||||||
| chr6:96583869 | C | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-19733C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583869 | |||||||
| chr6:96584074 | T | C | 1 | a0001c0004t0003g0254 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-12-19528T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584074 | |||||||
| chr6:96584110 | G | A | 1 | a0003c0003t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12-19492G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584110 | |||||||
| chr6:96584202 | A | G | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-19400A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584202 | |||||||
| chr6:96584435 | A | ATG | 47 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(44): Show |
62 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.-12-19143_-12-1914 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | ||||||
| chr6:96584435 | A | ATGTG | 9 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-19145_-12-1914 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | ||||||
| chr6:96584435 | ATGTGTG | A | 89 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(86): Show |
121 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-19147_-12-1914 others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | ||||||
| chr6:96584435 | ATGTGTGT others(19): Show |
A | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-19141_-12-1911 others(30): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | ||||||
| chr6:96584455 | G | T | 8 | a0001c0001t0002g0078 a0001c0001t0002g0102 a0001c0001t0004g0215 others(5): Show |
8 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-19147G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584455 | |||||||
| chr6:96584457 | GTGTT | G | 8 | a0001c0001t0002g0078 a0001c0001t0002g0102 a0001c0001t0004g0215 others(5): Show |
8 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-19141_-12-1913 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584457 | ||||||
| chr6:96584461 | T | G | 9 | a0001c0001t0004g0208 a0001c0001t0009g0063 a0001c0001t0009g0066 others(6): Show |
9 | HG00544.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-19141T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584461 | |||||||
| chr6:96584461 | T | TTG | 4 | a0002c0002t0001g0038 a0003c0003t0001g0004 a0003c0003t0001g0034 others(1): Show |
4 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-19115_-12-1911 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | ||||||
| chr6:96584461 | TTG | T | 3 | a0001c0001t0009g0064 a0002c0002t0011g0148 a0003c0003t0001g0175 |
3 | HG00733.hp2 HG01168.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12-19115_-12-1911 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | ||||||
| chr6:96584461 | TTGTGTGT others(3): Show |
T | 1 | a0002c0002t0001g0124 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-12-19123_-12-1911 others(14): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | ||||||
| chr6:96584463 | G | GTT | 5 | a0001c0001t0009g0063 a0001c0001t0009g0066 a0004c0005t0001g0065 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-19138_-12-1913 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584463 | ||||||
| chr6:96584463 | G | T | 3 | a0001c0001t0002g0040 a0001c0004t0003g0273 a0005c0008t0012g0068 |
4 | HG02257.hp1 HG02965.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-19139G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584463 | |||||||
| chr6:96584909 | G | T | 1 | a0002c0002t0001g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12-18693G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584909 | |||||||
| chr6:96585093 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12-18509C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585093 | |||||||
| chr6:96585321 | A | G | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-18281A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585321 | |||||||
| chr6:96585382 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12-18220T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585382 | |||||||
| chr6:96585385 | A | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(18): Show |
37 | HG00544.hp1 HG00621.hp2 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.-12-18217A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585385 | |||||||
| chr6:96585422 | A | G | 3 | a0003c0003t0004g0037 a0003c0003t0004g0179 a0003c0003t0004g0200 |
4 | HG01496.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-18180A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585422 | |||||||
| chr6:96585457 | A | G | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-18145A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585457 | |||||||
| chr6:96585494 | A | G | 48 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(45): Show |
63 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-12-18108A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585494 | |||||||
| chr6:96585904 | G | A | 93 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(90): Show |
116 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-12-17698G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585904 | |||||||
| chr6:96585937 | C | A | 1 | a0001c0001t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-17665C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585937 | |||||||
| chr6:96586228 | G | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-17374G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586228 | |||||||
| chr6:96586267 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-17335T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586267 | |||||||
| chr6:96586357 | T | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-17245T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586357 | |||||||
| chr6:96586450 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-17152A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586450 | |||||||
| chr6:96586454 | GTC | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-17144_-12-1714 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96586454 | ||||||
| chr6:96586598 | T | G | 1 | a0003c0003t0004g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12-17004T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586598 | |||||||
| chr6:96586839 | G | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-16763G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586839 | |||||||
| chr6:96586998 | C | T | 52 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(49): Show |
77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-12-16604C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586998 | |||||||
| chr6:96587038 | A | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-16564A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587038 | |||||||
| chr6:96587057 | C | A | 7 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(4): Show |
7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-16545C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587057 | |||||||
| chr6:96587219 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-12-16383T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587219 | |||||||
| chr6:96587245 | CAA | C | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-16356_-12-1635 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587245 | |||||||
| chr6:96587264 | A | G | 20 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0042 others(17): Show |
24 | HG00408.hp1 HG00544.hp2 HG02886.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-16338A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587264 | |||||||
| chr6:96587325 | C | T | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16277C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587325 | |||||||
| chr6:96587355 | A | G | 15 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0131 others(12): Show |
18 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-16247A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587355 | |||||||
| chr6:96587506 | T | TA | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16093dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96587506 | ||||||
| chr6:96587542 | C | T | 82 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(79): Show |
104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-16060C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587542 | |||||||
| chr6:96587568 | T | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-16034T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587568 | |||||||
| chr6:96587641 | C | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-15961C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587641 | |||||||
| chr6:96587780 | T | C | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15822T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587780 | |||||||
| chr6:96587856 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-15746G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587856 | |||||||
| chr6:96587892 | AG | A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-15707delG | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96587892 | ||||||
| chr6:96588019 | C | T | 1 | a0002c0002t0006g0168 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12-15583C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588019 | |||||||
| chr6:96588020 | G | A | 1 | a0001c0004t0003g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-15582G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588020 | |||||||
| chr6:96588119 | T | C | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-15483T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588119 | |||||||
| chr6:96588192 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(28): Show |
52 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-12-15410G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588192 | |||||||
| chr6:96588266 | A | G | 175 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(172): Show |
226 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.-12-15336A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588266 | |||||||
| chr6:96588280 | G | A | 1 | a0003c0003t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12-15322G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588280 | |||||||
| chr6:96588325 | C | T | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12-15277C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588325 | |||||||
| chr6:96588337 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-12-15265A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588337 | |||||||
| chr6:96588504 | T | G | 1 | a0001c0001t0009g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-15098T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588504 | |||||||
| chr6:96588534 | T | A | 1 | a0001c0001t0004g0218 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-12-15068T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588534 | |||||||
| chr6:96588589 | G | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15013G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588589 | |||||||
| chr6:96588590 | T | G | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15012T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588590 | |||||||
| chr6:96588663 | C | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-14939C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588663 | |||||||
| chr6:96588672 | A | C | 1 | a0003c0003t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-12-14930A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588672 | |||||||
| chr6:96588683 | T | C | 82 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(79): Show |
104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14919T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588683 | |||||||
| chr6:96588684 | T | A | 82 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(79): Show |
104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14918T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588684 | |||||||
| chr6:96588687 | G | A | 82 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(79): Show |
104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14915G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588687 | |||||||
| chr6:96588706 | T | A | 1 | a0002c0002t0001g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12-14896T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588706 | |||||||
| chr6:96588850 | TTAAA | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-14749_-12-1474 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96588850 | ||||||
| chr6:96588881 | T | TA | 84 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(81): Show |
105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-12-14712dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96588881 | ||||||
| chr6:96589067 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-12-14535T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589067 | |||||||
| chr6:96589465 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0005g0035 |
2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-12-14137T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589465 | |||||||
| chr6:96589607 | T | C | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-13995T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589607 | |||||||
| chr6:96589685 | T | C | 3 | a0001c0001t0004g0017 a0001c0001t0004g0210 a0001c0001t0004g0211 |
5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-13917T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589685 | |||||||
| chr6:96589797 | T | C | 1 | a0002c0002t0001g0151 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-12-13805T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589797 | |||||||
| chr6:96589801 | C | G | 3 | a0002c0002t0001g0009 a0002c0002t0001g0031 a0002c0002t0001g0161 |
7 | HG00733.hp1 HG01256.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-13801C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589801 | |||||||
| chr6:96589984 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-13618G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589984 | |||||||
| chr6:96590342 | A | T | 1 | a0002c0002t0001g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12-13260A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590342 | |||||||
| chr6:96590527 | G | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-13075G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590527 | |||||||
| chr6:96590817 | C | A | 3 | a0001c0004t0003g0047 a0001c0004t0003g0252 a0001c0004t0003g0267 |
4 | HG02486.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-12785C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590817 | |||||||
| chr6:96590981 | G | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-12621G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590981 | |||||||
| chr6:96591006 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-12596T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591006 | |||||||
| chr6:96591072 | C | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-12-12530C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591072 | |||||||
| chr6:96591080 | T | G | 1 | a0001c0001t0007g0053 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12-12522T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591080 | |||||||
| chr6:96591123 | T | C | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-12479T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591123 | |||||||
| chr6:96591141 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0021 a0001c0001t0002g0099 |
6 | HG00621.hp2 HG02165.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-12461G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591141 | |||||||
| chr6:96591428 | C | T | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-12174C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591428 | |||||||
| chr6:96591462 | A | G | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-12140A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591462 | |||||||
| chr6:96591498 | T | G | 1 | a0003c0003t0004g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-12-12104T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591498 | |||||||
| chr6:96591545 | A | T | 43 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-12-12057A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591545 | |||||||
| chr6:96591638 | C | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11964C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591638 | |||||||
| chr6:96591745 | G | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-11857G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591745 | |||||||
| chr6:96591788 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-11814C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591788 | |||||||
| chr6:96591789 | A | G | 92 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(89): Show |
114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-11813A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591789 | |||||||
| chr6:96591844 | C | G | 29 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(26): Show |
41 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-12-11758C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591844 | |||||||
| chr6:96591865 | G | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-11737G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591865 | |||||||
| chr6:96591881 | T | C | 92 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(89): Show |
114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-11721T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591881 | |||||||
| chr6:96591887 | G | A | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-11715G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591887 | |||||||
| chr6:96591942 | G | A | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12-11660G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591942 | |||||||
| chr6:96591945 | T | C | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-12-11657T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591945 | |||||||
| chr6:96591973 | T | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-11629T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591973 | |||||||
| chr6:96591981 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-11621A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591981 | |||||||
| chr6:96592068 | C | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0002c0002t0001g0197 |
3 | NA18984.hp1 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-12-11534C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592068 | |||||||
| chr6:96592120 | A | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-11482A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592120 | |||||||
| chr6:96592138 | T | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11464T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592138 | |||||||
| chr6:96592143 | G | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11459G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592143 | |||||||
| chr6:96592177 | C | G | 2 | a0002c0002t0001g0132 a0002c0002t0001g0133 |
2 | NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12-11425C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592177 | |||||||
| chr6:96592189 | C | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(65): Show |
95 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-12-11413C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592189 | |||||||
| chr6:96592208 | T | C | 2 | a0001c0001t0021g0074 a0001c0004t0003g0048 |
3 | HG02257.hp2 HG02293.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-12-11394T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592208 | |||||||
| chr6:96592252 | G | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11350G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592252 | |||||||
| chr6:96592369 | C | T | 1 | a0003c0003t0001g0134 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-12-11233C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592369 | |||||||
| chr6:96592372 | C | A | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-11230C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592372 | |||||||
| chr6:96592376 | C | T | 1 | a0001c0001t0009g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-11226C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592376 | |||||||
| chr6:96592385 | G | A | 1 | a0003c0003t0001g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-12-11217G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592385 | |||||||
| chr6:96592418 | T | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0242 |
2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12-11184T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592418 | |||||||
| chr6:96592466 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11136A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592466 | |||||||
| chr6:96592478 | C | A | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-11124C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592478 | |||||||
| chr6:96592597 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-12-11005A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592597 | |||||||
| chr6:96592640 | T | C | 2 | a0001c0004t0003g0259 a0001c0004t0003g0260 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-10962T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592640 | |||||||
| chr6:96592797 | C | T | 1 | a0001c0001t0021g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-10805C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592797 | |||||||
| chr6:96592798 | G | A | 27 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(24): Show |
32 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-10804G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592798 | |||||||
| chr6:96592833 | G | T | 1 | a0001c0001t0004g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12-10769G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592833 | |||||||
| chr6:96592838 | T | C | 1 | a0001c0004t0003g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-12-10764T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592838 | |||||||
| chr6:96592840 | G | A | 2 | a0002c0002t0001g0153 a0007c0011t0001g0154 |
2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-12-10762G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592840 | |||||||
| chr6:96593016 | T | G | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-10586T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593016 | |||||||
| chr6:96593018 | T | C | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-10584T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593018 | |||||||
| chr6:96593470 | G | C | 1 | a0002c0002t0001g0149 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-12-10132G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593470 | |||||||
| chr6:96593520 | A | G | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-10082A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593520 | |||||||
| chr6:96593706 | A | T | 1 | a0001c0001t0004g0042 | 2 | NA18963.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-12-9896A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593706 | |||||||
| chr6:96593759 | C | T | 40 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(37): Show |
48 | HG00408.hp1 HG00544.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-12-9843C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593759 | |||||||
| chr6:96593798 | G | A | 1 | a0002c0002t0001g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-12-9804G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593798 | |||||||
| chr6:96593955 | T | G | 1 | a0002c0002t0006g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-12-9647T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593955 | |||||||
| chr6:96594102 | C | T | 1 | a0006c0009t0004g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-9500C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594102 | |||||||
| chr6:96594224 | AATTTATA others(11): Show |
A | 1 | a0003c0003t0001g0281 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12-9375_-12-9358d others(20): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594224 | ||||||
| chr6:96594226 | TTTATA | T | 3 | a0001c0001t0004g0020 a0003c0003t0001g0277 a0003c0003t0004g0200 |
3 | HG02886.hp2 NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-9374_-12-9370d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594226 | ||||||
| chr6:96594227 | T | TTA | 26 | a0001c0001t0004g0018 a0001c0001t0004g0210 a0001c0001t0004g0222 others(23): Show |
26 | HG00408.hp2 HG00621.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-12-9329_-12-9328d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | T | TTATA | 6 | a0001c0001t0004g0221 a0001c0001t0004g0232 a0001c0001t0009g0206 others(3): Show |
6 | HG02109.hp1 HG02970.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9331_-12-9328d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTA | T | 41 | a0001c0001t0002g0104 a0001c0001t0004g0017 a0001c0001t0004g0042 others(38): Show |
46 | HG00673.hp2 HG00733.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-12-9329_-12-9328d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATA | T | 28 | a0001c0001t0002g0040 a0001c0001t0004g0060 a0001c0001t0004g0061 others(25): Show |
34 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-9331_-12-9328d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATA | T | 18 | a0001c0001t0002g0088 a0001c0001t0004g0020 a0001c0001t0004g0220 others(15): Show |
18 | HG01070.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-9333_-12-9328d others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(1): Show |
T | 6 | a0001c0004t0003g0051 a0002c0002t0001g0035 a0002c0002t0005g0035 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9335_-12-9328d others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(3): Show |
T | 15 | a0001c0001t0002g0008 a0001c0001t0002g0027 a0001c0001t0002g0077 others(12): Show |
16 | HG00597.hp1 HG00673.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-9337_-12-9328d others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(5): Show |
T | 16 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(13): Show |
18 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-9339_-12-9328d others(14): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(7): Show |
T | 29 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(26): Show |
38 | HG00423.hp1 HG01074.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12-9341_-12-9328d others(16): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(9): Show |
T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(55): Show |
77 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-12-9343_-12-9328d others(18): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(11): Show |
T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0100 a0002c0002t0001g0009 others(1): Show |
4 | HG00280.hp1 HG03239.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-9345_-12-9328d others(20): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(13): Show |
T | 12 | a0001c0001t0002g0062 a0001c0001t0002g0242 a0001c0001t0004g0207 others(9): Show |
14 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-9347_-12-9328d others(22): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(15): Show |
T | 8 | a0001c0001t0004g0227 a0002c0002t0001g0015 a0002c0002t0006g0015 others(5): Show |
9 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-9349_-12-9328d others(24): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594227 | TTATATAT others(17): Show |
T | 2 | a0002c0002t0001g0139 a0004c0013t0018g0052 |
2 | HG01952.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-12-9351_-12-9328d others(26): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | ||||||
| chr6:96594229 | A | T | 1 | a0002c0002t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-9373A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594229 | |||||||
| chr6:96594245 | A | T | 1 | a0001c0001t0002g0241 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12-9357A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594245 | |||||||
| chr6:96594259 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9343A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594259 | |||||||
| chr6:96594261 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-9337_-12-9324d others(16): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594261 | ||||||
| chr6:96594271 | A | T | 48 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(45): Show |
63 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-12-9331A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594271 | |||||||
| chr6:96594273 | A | G | 1 | a0003c0003t0001g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12-9329A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594273 | |||||||
| chr6:96594582 | T | C | 1 | a0003c0003t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12-9020T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594582 | |||||||
| chr6:96594616 | T | C | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-8986T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594616 | |||||||
| chr6:96594743 | T | TA | 10 | a0001c0004t0003g0057 a0001c0004t0003g0245 a0001c0004t0003g0246 others(7): Show |
10 | NA18944.hp1 NA18957.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-8858dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594743 | ||||||
| chr6:96594971 | T | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-8631T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594971 | |||||||
| chr6:96595041 | G | A | 1 | a0003c0003t0001g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12-8561G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595041 | |||||||
| chr6:96595094 | G | T | 33 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(30): Show |
39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-12-8508G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595094 | |||||||
| chr6:96595149 | C | G | 92 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(89): Show |
114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-8453C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595149 | |||||||
| chr6:96595167 | T | C | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-8435T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595167 | |||||||
| chr6:96595276 | G | A | 1 | a0001c0004t0003g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-12-8326G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595276 | |||||||
| chr6:96595394 | C | T | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-8208C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595394 | |||||||
| chr6:96595565 | A | C | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-8037A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595565 | |||||||
| chr6:96595627 | C | T | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-7975C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595627 | |||||||
| chr6:96595987 | G | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-7615G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595987 | |||||||
| chr6:96596018 | GA | G | 3 | a0001c0001t0012g0072 a0001c0001t0013g0073 a0001c0001t0014g0071 |
3 | HG02886.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-12-7583delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596018 | |||||||
| chr6:96596349 | A | G | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-7253A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596349 | |||||||
| chr6:96596449 | A | T | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-7153A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596449 | |||||||
| chr6:96596559 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-7043C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596559 | |||||||
| chr6:96596601 | T | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-7001T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596601 | |||||||
| chr6:96596613 | CT | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-6980delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96596613 | ||||||
| chr6:96596724 | G | A | 29 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(26): Show |
35 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-12-6878G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596724 | |||||||
| chr6:96596774 | A | C | 1 | a0001c0001t0009g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-6828A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596774 | |||||||
| chr6:96596908 | G | A | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-6694G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596908 | |||||||
| chr6:96596928 | ACT | A | 3 | a0002c0002t0001g0016 a0002c0002t0001g0131 a0002c0002t0001g0180 |
5 | HG02015.hp1 HG02027.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-6660_-12-6659d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96596928 | ||||||
| chr6:96596941 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-6661C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596941 | |||||||
| chr6:96596955 | C | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-6647C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596955 | |||||||
| chr6:96596981 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12-6621C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596981 | |||||||
| chr6:96597366 | A | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6236A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597366 | |||||||
| chr6:96597367 | C | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6235C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597367 | |||||||
| chr6:96597374 | A | AC | 153 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(150): Show |
200 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-12-6228_-12-6227i others(3): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597374 | |||||||
| chr6:96597374 | A | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6228A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597374 | |||||||
| chr6:96597429 | A | G | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(65): Show |
95 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-12-6173A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597429 | |||||||
| chr6:96597458 | G | A | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-6144G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597458 | |||||||
| chr6:96597501 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12-6101T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597501 | |||||||
| chr6:96597605 | C | G | 1 | a0002c0002t0001g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-12-5997C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597605 | |||||||
| chr6:96597672 | C | G | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5930C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597672 | |||||||
| chr6:96597888 | C | T | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-5714C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597888 | |||||||
| chr6:96597965 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5637C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597965 | |||||||
| chr6:96598038 | A | T | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5564A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598038 | |||||||
| chr6:96598088 | G | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-5514G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598088 | |||||||
| chr6:96598099 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12-5503C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598099 | |||||||
| chr6:96598189 | C | T | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5413C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598189 | |||||||
| chr6:96598249 | T | C | 1 | a0001c0001t0002g0022 | 2 | NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-12-5353T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598249 | |||||||
| chr6:96598388 | G | C | 10 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(7): Show |
10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-5214G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598388 | |||||||
| chr6:96598578 | G | C | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5024G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598578 | |||||||
| chr6:96598693 | A | G | 1 | a0002c0002t0001g0159 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-12-4909A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598693 | |||||||
| chr6:96598701 | A | C | 1 | a0002c0002t0015g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-12-4901A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598701 | |||||||
| chr6:96598733 | T | A | 1 | a0001c0001t0004g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12-4869T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598733 | |||||||
| chr6:96598776 | G | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(65): Show |
95 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-12-4826G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598776 | |||||||
| chr6:96598894 | C | T | 1 | a0001c0004t0003g0272 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-12-4708C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598894 | |||||||
| chr6:96599042 | AAATGTTA others(2): Show |
A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-4550_-12-4542d others(11): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599042 | ||||||
| chr6:96599141 | C | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-4461C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599141 | |||||||
| chr6:96599160 | G | C | 10 | a0001c0001t0004g0043 a0001c0001t0004g0228 a0001c0001t0004g0229 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-4442G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599160 | |||||||
| chr6:96599191 | C | CT | 8 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(5): Show |
8 | HG01109.hp2 HG02258.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-4390dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | ||||||
| chr6:96599191 | CT | C | 148 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(145): Show |
194 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.-12-4390delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | ||||||
| chr6:96599191 | CTT | C | 11 | a0001c0001t0002g0026 a0001c0001t0002g0087 a0001c0001t0002g0089 others(8): Show |
12 | HG00423.hp1 HG01517.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12-4391_-12-4390d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | ||||||
| chr6:96599232 | G | T | 1 | a0006c0009t0004g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-4370G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599232 | |||||||
| chr6:96599258 | C | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-4344C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599258 | |||||||
| chr6:96599270 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-4332A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599270 | |||||||
| chr6:96599324 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12-4278T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599324 | |||||||
| chr6:96599342 | T | C | 7 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(4): Show |
9 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-4260T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599342 | |||||||
| chr6:96599382 | C | G | 1 | a0001c0004t0003g0263 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12-4220C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599382 | |||||||
| chr6:96599446 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-4156T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599446 | |||||||
| chr6:96599470 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-4132C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599470 | |||||||
| chr6:96599474 | C | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-4128C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599474 | |||||||
| chr6:96599575 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-12-4027A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599575 | |||||||
| chr6:96599687 | C | T | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-3915C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599687 | |||||||
| chr6:96599749 | G | A | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-3853G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599749 | |||||||
| chr6:96599761 | A | C | 2 | a0003c0003t0001g0144 a0003c0003t0001g0178 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-12-3841A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599761 | |||||||
| chr6:96599870 | T | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-3732T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599870 | |||||||
| chr6:96600088 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-12-3514G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600088 | |||||||
| chr6:96600126 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-12-3476A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600126 | |||||||
| chr6:96600242 | T | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-3360T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600242 | |||||||
| chr6:96600364 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-12-3238C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600364 | |||||||
| chr6:96600499 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12-3103C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600499 | |||||||
| chr6:96600549 | T | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-3053T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600549 | |||||||
| chr6:96600593 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0060 a0001c0001t0004g0061 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-3009G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600593 | |||||||
| chr6:96600612 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-12-2990T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600612 | |||||||
| chr6:96600632 | T | C | 6 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 others(3): Show |
6 | HG00408.hp1 HG00544.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-2970T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600632 | |||||||
| chr6:96600649 | A | T | 1 | a0001c0004t0003g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12-2953A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600649 | |||||||
| chr6:96601050 | C | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2552C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601050 | |||||||
| chr6:96601106 | T | C | 185 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(182): Show |
236 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-12-2496T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601106 | |||||||
| chr6:96601157 | A | T | 2 | a0001c0001t0009g0064 a0005c0008t0012g0068 |
2 | HG00733.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-12-2445A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601157 | |||||||
| chr6:96601283 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12-2319G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601283 | |||||||
| chr6:96601315 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-2287T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601315 | |||||||
| chr6:96601322 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2280G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601322 | |||||||
| chr6:96601414 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2188A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601414 | |||||||
| chr6:96601440 | G | A | 3 | a0001c0001t0004g0017 a0001c0001t0004g0210 a0001c0001t0004g0211 |
5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-2162G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601440 | |||||||
| chr6:96601478 | A | G | 2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-2124A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601478 | |||||||
| chr6:96601656 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1946G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601656 | |||||||
| chr6:96601710 | C | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1892C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601710 | |||||||
| chr6:96601711 | G | A | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-1891G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601711 | |||||||
| chr6:96601777 | T | G | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1825T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601777 | |||||||
| chr6:96601783 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12-1819G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601783 | |||||||
| chr6:96602023 | C | A | 43 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-12-1579C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602023 | |||||||
| chr6:96602228 | C | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1374C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602228 | |||||||
| chr6:96602299 | T | C | 1 | a0004c0005t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-1303T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602299 | |||||||
| chr6:96602387 | A | G | 4 | a0002c0002t0001g0016 a0002c0002t0001g0131 a0002c0002t0001g0167 others(1): Show |
6 | HG02015.hp1 HG02027.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-1215A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602387 | |||||||
| chr6:96602389 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-12-1213T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602389 | |||||||
| chr6:96602422 | G | GTTCCTTT others(3): Show |
1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1178_-12-1177i others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602422 | ||||||
| chr6:96602425 | T | C | 9 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(6): Show |
9 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-1177T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602425 | |||||||
| chr6:96602426 | C | CT | 58 | a0001c0001t0004g0229 a0001c0001t0004g0232 a0001c0001t0004g0233 others(55): Show |
73 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-12-1138dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | C | CTT | 22 | a0002c0002t0001g0030 a0002c0002t0001g0139 a0002c0002t0001g0159 others(19): Show |
24 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12-1139_-12-1138d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | C | T | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1176C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602426 | |||||||
| chr6:96602426 | CT | C | 6 | a0001c0001t0012g0072 a0001c0001t0013g0073 a0001c0001t0021g0074 others(3): Show |
6 | HG01074.hp1 HG01167.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1138delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTT | C | 13 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-1142_-12-1138d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTT | C | 34 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(31): Show |
47 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-12-1143_-12-1138d others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT | C | 74 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0021 others(71): Show |
105 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-12-1144_-12-1138d others(9): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT others(1): Show |
C | 12 | a0001c0001t0002g0024 a0001c0001t0002g0076 a0001c0001t0002g0083 others(9): Show |
14 | HG01081.hp1 HG01169.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12-1145_-12-1138d others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT others(4): Show |
C | 1 | a0003c0003t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-12-1148_-12-1138d others(13): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0009g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12-1157_-12-1138d others(22): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT others(14): Show |
C | 8 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0004c0005t0001g0065 others(5): Show |
8 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1158_-12-1138d others(23): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602426 | CTTTTTTT others(15): Show |
C | 1 | a0003c0003t0010g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-12-1159_-12-1138d others(24): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | ||||||
| chr6:96602432 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-12-1170T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602432 | |||||||
| chr6:96602434 | T | C | 8 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(5): Show |
8 | HG03453.hp2 NA18906.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-1168T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602434 | |||||||
| chr6:96602435 | T | C | 19 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(16): Show |
25 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12-1167T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602435 | |||||||
| chr6:96602436 | T | C | 7 | a0001c0001t0004g0060 a0001c0001t0004g0216 a0001c0004t0003g0044 others(4): Show |
8 | HG01433.hp2 HG02622.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1166T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602436 | |||||||
| chr6:96602437 | T | C | 36 | a0001c0001t0004g0215 a0001c0001t0004g0225 a0001c0004t0003g0005 others(33): Show |
48 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12-1165T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602437 | |||||||
| chr6:96602438 | T | C | 4 | a0001c0004t0003g0045 a0001c0004t0003g0259 a0001c0004t0003g0270 others(1): Show |
5 | HG01081.hp1 HG01256.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-1164T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602438 | |||||||
| chr6:96602441 | T | C | 1 | a0001c0004t0003g0253 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-12-1161T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602441 | |||||||
| chr6:96602488 | CCAGGCTG others(67): Show |
C | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1110_-12-1037d others(76): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602488 | ||||||
| chr6:96602506 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12-1096G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602506 | |||||||
| chr6:96602520 | C | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1082C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602520 | |||||||
| chr6:96602927 | A | G | 2 | a0003c0003t0001g0125 a0003c0003t0001g0126 |
2 | HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-12-675A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602927 | |||||||
| chr6:96602983 | CAG | C | 3 | a0001c0001t0002g0025 a0001c0001t0002g0088 a0001c0001t0002g0093 |
4 | HG02074.hp2 HG02083.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-615_-12-614del others(2): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602983 | ||||||
| chr6:96603084 | T | C | 1 | a0002c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-518T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96603084 | |||||||
| chr6:96603591 | G | T | 1 | a0006c0009t0004g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-11G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96603591 | |||||||
| chr6:96604037 | A | C | 2 | a0002c0002t0001g0155 a0002c0002t0001g0172 |
2 | NA18957.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.159+265A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604037 | |||||||
| chr6:96604074 | C | T | 1 | a0003c0003t0001g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.159+302C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604074 | |||||||
| chr6:96604227 | T | G | 31 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(28): Show |
37 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+455T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604227 | |||||||
| chr6:96604239 | C | G | 5 | a0001c0001t0002g0026 a0001c0001t0002g0087 a0001c0001t0002g0089 others(2): Show |
6 | HG00423.hp1 NA18967.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+467C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604239 | |||||||
| chr6:96604242 | ATTCT | A | 7 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(4): Show |
7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-486_160-483del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604242 | ||||||
| chr6:96604288 | C | T | 43 | a0001c0001t0004g0215 a0001c0001t0004g0225 a0001c0004t0003g0005 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.160-462C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604288 | |||||||
| chr6:96604307 | T | TTC | 27 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(24): Show |
31 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.160-419_160-418dup others(2): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604307 | ||||||
| chr6:96604307 | TTCTC | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-421_160-418del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604307 | ||||||
| chr6:96604377 | T | C | 1 | a0004c0005t0004g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160-373T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604377 | |||||||
| chr6:96604410 | G | A | 45 | a0001c0001t0004g0215 a0001c0001t0004g0225 a0001c0004t0003g0005 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.160-340G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604410 | |||||||
| chr6:96604476 | A | G | 1 | a0001c0001t0004g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.160-274A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604476 | |||||||
| chr6:96605029 | A | C | 9 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(6): Show |
9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334+105A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605029 | |||||||
| chr6:96605229 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334+305C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605229 | |||||||
| chr6:96605277 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.334+353T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605277 | |||||||
| chr6:96605327 | G | A | 1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+403G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605327 | |||||||
| chr6:96605423 | A | G | 1 | a0003c0003t0001g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.335-479A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605423 | |||||||
| chr6:96605605 | A | C | 33 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(30): Show |
39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.335-297A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605605 | |||||||
| chr6:96605638 | C | T | 42 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(39): Show |
56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-264C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605638 | |||||||
| chr6:96605725 | AT | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-168delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 96605725 | ||||||
| chr6:96606155 | T | C | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.504+84T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606155 | |||||||
| chr6:96606234 | G | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+163G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606234 | |||||||
| chr6:96606253 | T | C | 1 | a0003c0003t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.504+182T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606253 | |||||||
| chr6:96606288 | T | A | 3 | a0001c0001t0004g0017 a0001c0001t0004g0210 a0001c0001t0004g0211 |
5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+217T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606288 | |||||||
| chr6:96606342 | T | G | 33 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(30): Show |
39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+271T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606342 | |||||||
| chr6:96606343 | T | G | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+272T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606343 | |||||||
| chr6:96606345 | G | T | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+274G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606345 | |||||||
| chr6:96606382 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.504+311C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606382 | |||||||
| chr6:96606387 | T | A | 33 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(30): Show |
39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+316T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606387 | |||||||
| chr6:96606438 | G | T | 43 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.504+367G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606438 | |||||||
| chr6:96606475 | C | G | 1 | a0003c0003t0004g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.504+404C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606475 | |||||||
| chr6:96606497 | G | A | 1 | a0002c0002t0004g0142 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.504+426G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606497 | |||||||
| chr6:96606499 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+428G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606499 | |||||||
| chr6:96606509 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+438G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606509 | |||||||
| chr6:96606542 | G | C | 2 | a0004c0005t0001g0067 a0004c0005t0001g0069 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.504+471G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606542 | |||||||
| chr6:96606617 | A | G | 158 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(155): Show |
207 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.504+546A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606617 | |||||||
| chr6:96606940 | T | C | 33 | a0001c0001t0002g0062 a0001c0001t0002g0240 a0001c0001t0002g0241 others(30): Show |
39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+869T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606940 | |||||||
| chr6:96607041 | T | C | 1 | a0001c0004t0003g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.504+970T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607041 | |||||||
| chr6:96607206 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.504+1135G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607206 | |||||||
| chr6:96607286 | T | TTCAAAGT others(830): Show |
2 | a0005c0006t0004g0243 a0005c0006t0004g0244 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.504+1229_504+1230i others(839): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | ||||||
| chr6:96607286 | T | TTCAAAGT others(837): Show |
1 | a0001c0001t0009g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.504+1229_504+1230i others(846): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | ||||||
| chr6:96607286 | T | TTCAAAGT others(836): Show |
2 | a0001c0001t0009g0066 a0004c0005t0001g0065 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.504+1229_504+1230i others(845): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | ||||||
| chr6:96607286 | T | TTCAAAGT others(837): Show |
4 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0004c0005t0001g0067 others(1): Show |
4 | HG00733.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1229_504+1230i others(846): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | ||||||
| chr6:96607406 | T | TAC | 47 | a0001c0001t0012g0072 a0001c0001t0013g0073 a0001c0001t0014g0071 others(44): Show |
62 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1354_504+1355d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | ||||||
| chr6:96607406 | TAC | T | 7 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+1354_504+1355d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | ||||||
| chr6:96607406 | TACACACA others(3): Show |
T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.504+1346_504+1355d others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | ||||||
| chr6:96607587 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.504+1516A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607587 | |||||||
| chr6:96607987 | C | A | 1 | a0002c0002t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.504+1916C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607987 | |||||||
| chr6:96608169 | C | T | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+2098C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608169 | |||||||
| chr6:96608178 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+2107G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608178 | |||||||
| chr6:96608379 | T | C | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.505-2193T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608379 | |||||||
| chr6:96608529 | G | A | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | HG01168.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.505-2043G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608529 | |||||||
| chr6:96608547 | A | G | 1 | a0001c0001t0009g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.505-2025A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608547 | |||||||
| chr6:96609103 | C | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(155): Show |
207 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.505-1469C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609103 | |||||||
| chr6:96609511 | T | A | 6 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(3): Show |
6 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1061T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609511 | |||||||
| chr6:96609582 | C | G | 1 | a0002c0002t0001g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.505-990C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609582 | |||||||
| chr6:96609787 | G | A | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505-785G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609787 | |||||||
| chr6:96609868 | G | A | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-704G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609868 | |||||||
| chr6:96609949 | G | A | 6 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(3): Show |
6 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-623G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609949 | |||||||
| chr6:96609953 | G | A | 1 | a0002c0002t0004g0142 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.505-619G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609953 | |||||||
| chr6:96610064 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0084 |
3 | NA19063.hp2 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.505-508C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610064 | |||||||
| chr6:96610268 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-304A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610268 | |||||||
| chr6:96610274 | T | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(52): Show |
81 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.505-298T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610274 | |||||||
| chr6:96610476 | T | A | 1 | a0002c0002t0001g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505-96T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610476 | |||||||
| chr6:96610836 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+78A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610836 | |||||||
| chr6:96610862 | C | T | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.691+104C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610862 | |||||||
| chr6:96610883 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+125A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610883 | |||||||
| chr6:96610921 | C | T | 3 | a0003c0003t0001g0276 a0003c0003t0001g0278 a0003c0003t0001g0280 |
3 | HG00741.hp2 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+163C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610921 | |||||||
| chr6:96610954 | T | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0124 |
3 | NA18951.hp2 NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.691+196T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610954 | |||||||
| chr6:96611055 | T | C | 61 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(58): Show |
70 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.691+297T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611055 | |||||||
| chr6:96611068 | G | A | 6 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.691+310G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611068 | |||||||
| chr6:96611086 | C | T | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.691+328C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611086 | |||||||
| chr6:96611249 | T | C | 44 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(41): Show |
52 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+491T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611249 | |||||||
| chr6:96611285 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+527G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611285 | |||||||
| chr6:96611556 | A | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+798A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611556 | |||||||
| chr6:96611578 | C | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+820C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611578 | |||||||
| chr6:96611668 | C | T | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+910C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611668 | |||||||
| chr6:96611694 | T | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+936T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611694 | |||||||
| chr6:96611697 | G | A | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+939G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611697 | |||||||
| chr6:96611790 | A | G | 147 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(144): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.691+1032A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611790 | |||||||
| chr6:96611893 | A | C | 147 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(144): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.691+1135A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611893 | |||||||
| chr6:96612078 | C | T | 6 | a0002c0002t0001g0137 a0002c0002t0001g0143 a0002c0002t0001g0155 others(3): Show |
6 | NA18948.hp1 NA18957.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.691+1320C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612078 | |||||||
| chr6:96612248 | G | A | 97 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(94): Show |
119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.691+1490G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612248 | |||||||
| chr6:96612321 | C | A | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.691+1563C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612321 | |||||||
| chr6:96612349 | T | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0124 |
3 | NA18951.hp2 NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.691+1591T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612349 | |||||||
| chr6:96612408 | C | T | 1 | a0002c0002t0004g0142 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691+1650C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612408 | |||||||
| chr6:96612443 | A | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(54): Show |
83 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.691+1685A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612443 | |||||||
| chr6:96612657 | T | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+1899T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612657 | |||||||
| chr6:96612812 | C | A | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
153 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.691+2054C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612812 | |||||||
| chr6:96612823 | T | A | 1 | a0001c0001t0004g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.691+2065T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612823 | |||||||
| chr6:96612823 | T | C | 1 | a0003c0003t0001g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.691+2065T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612823 | |||||||
| chr6:96612889 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.691+2131G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612889 | |||||||
| chr6:96613095 | G | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+2337G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613095 | |||||||
| chr6:96613183 | G | C | 1 | a0002c0002t0001g0189 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.691+2425G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613183 | |||||||
| chr6:96613224 | TTTTA | T | 154 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(151): Show |
202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.692-2381_692-2378d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 96613224 | ||||||
| chr6:96613260 | T | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-2349T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613260 | |||||||
| chr6:96613283 | C | T | 156 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(153): Show |
205 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.692-2326C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613283 | |||||||
| chr6:96613293 | C | G | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-2316C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613293 | |||||||
| chr6:96613296 | G | C | 9 | a0001c0001t0009g0063 a0001c0001t0009g0064 a0001c0001t0009g0066 others(6): Show |
9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.692-2313G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613296 | |||||||
| chr6:96613349 | A | T | 1 | a0001c0004t0003g0254 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.692-2260A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613349 | |||||||
| chr6:96613436 | G | A | 3 | a0004c0005t0004g0041 a0004c0010t0022g0059 a0004c0013t0018g0052 |
4 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-2173G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613436 | |||||||
| chr6:96613611 | A | C | 2 | a0001c0001t0002g0104 a0004c0010t0022g0059 |
2 | HG03453.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.692-1998A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613611 | |||||||
| chr6:96613619 | T | C | 1 | a0001c0004t0003g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.692-1990T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613619 | |||||||
| chr6:96613648 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.692-1961C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613648 | |||||||
| chr6:96613874 | C | T | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1735C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613874 | |||||||
| chr6:96613914 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.692-1695C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613914 | |||||||
| chr6:96614064 | T | C | 41 | a0001c0004t0003g0005 a0001c0004t0003g0011 a0001c0004t0003g0044 others(38): Show |
55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.692-1545T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614064 | |||||||
| chr6:96614082 | A | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1527A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614082 | |||||||
| chr6:96614149 | T | A | 17 | a0001c0001t0004g0018 a0001c0001t0004g0042 a0001c0001t0004g0207 others(14): Show |
20 | HG00408.hp1 HG00544.hp2 HG03490.hp1 others(17): Show |
intron_variant | MODIFIER | c.692-1460T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614149 | |||||||
| chr6:96614151 | C | T | 1 | a0002c0002t0001g0159 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.692-1458C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614151 | |||||||
| chr6:96614152 | C | T | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1457C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614152 | |||||||
| chr6:96614241 | ATAAT | A | 46 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(43): Show |
61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.692-1365_692-1362d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 96614241 | ||||||
| chr6:96614301 | C | A | 1 | a0004c0013t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.692-1308C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614301 | |||||||
| chr6:96614344 | T | C | 5 | a0001c0001t0007g0019 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-1265T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614344 | |||||||
| chr6:96614355 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.692-1254C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614355 | |||||||
| chr6:96614444 | G | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1165G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614444 | |||||||
| chr6:96614630 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-979G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614630 | |||||||
| chr6:96614677 | A | G | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-932A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614677 | |||||||
| chr6:96614687 | G | C | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-922G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614687 | |||||||
| chr6:96614736 | C | T | 3 | a0001c0001t0004g0209 a0001c0001t0004g0224 a0001c0001t0004g0227 |
3 | NA18970.hp2 NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.692-873C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614736 | |||||||
| chr6:96614748 | C | T | 1 | a0002c0002t0005g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.692-861C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614748 | |||||||
| chr6:96614756 | A | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.692-853A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614756 | |||||||
| chr6:96614832 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.692-777A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614832 | |||||||
| chr6:96614916 | G | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0042 others(17): Show |
24 | HG00408.hp1 HG00544.hp2 HG02886.hp2 others(21): Show |
intron_variant | MODIFIER | c.692-693G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614916 | |||||||
| chr6:96614959 | C | T | 154 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(151): Show |
202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.692-650C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614959 | |||||||
| chr6:96614989 | C | A | 1 | a0007c0011t0001g0154 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.692-620C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614989 | |||||||
| chr6:96614990 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-619G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614990 | |||||||
| chr6:96614998 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-611G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614998 | |||||||
| chr6:96615029 | GTTAT | G | 154 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(151): Show |
202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.692-579_692-576del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615029 | |||||||
| chr6:96615129 | C | G | 154 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(151): Show |
202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.692-480C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615129 | |||||||
| chr6:96615216 | T | C | 1 | a0006c0009t0004g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.692-393T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615216 | |||||||
| chr6:96615273 | C | T | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-336C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615273 | |||||||
| chr6:96615353 | A | G | 1 | a0001c0001t0009g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-256A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615353 | |||||||
| chr6:96615554 | G | A | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-55G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615554 | |||||||
| chr6:96615563 | G | C | 1 | a0004c0010t0022g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-46G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615563 |