Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2184 |
| ensemblid | ENSG00000103876.14 |
| hgncid | 3579 |
| symbol | FAH |
| name | fumarylacetoacetate hydrolase |
| refseq_nuc | NM_000137.4 |
| refseq_prot | NP_000128.1 |
| ensembl_nuc | ENST00000561421.6 |
| ensembl_prot | ENSP00000453347.2 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 80152999 |
| end | 80186349 |
| strand | + |
| ver | v1.2 |
| region | chr15:80152999-80186349 |
| region5000 | chr15:80147999-80191349 |
| regionname0 | FAH_chr15_80152999_80186349 |
| regionname5000 | FAH_chr15_80147999_80191349 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 419 | 411 | 88 | 76 | 184 | 16 | 45 | 147 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0002 | 0/0 | 419 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0003 | 0/0 | 419 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0004 | 0/0 | 419 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0005 | 0/0 | 419 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0006 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0007 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0008 | 0/0 | 419 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0009 | 0/0 | 419 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| a0010 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | MSFIP others(414): Show |
chr15 | 80147999 | 80191349 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1257 | 349 | 76 | 68 | 155 | 16 | 32 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0002 | 0/0 | 1257 | 24 | 2 | 3 | 15 | 0 | 4 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0003 | 0/0 | 1257 | 15 | 5 | 4 | 3 | 0 | 3 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0004 | 0/0 | 1257 | 11 | 0 | 0 | 11 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0005 | 0/0 | 1257 | 4 | 3 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0006 | 0/0 | 1257 | 4 | 0 | 0 | 0 | 0 | 4 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0011 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0012 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0014 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0001c0018 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0002c0007 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0003c0008 | 0/0 | 1257 | 3 | 1 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0004c0009 | 0/0 | 1257 | 3 | 0 | 0 | 3 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0005c0010 | 0/0 | 1257 | 2 | 0 | 1 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0006c0015 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0007c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0008c0016 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0009c0017 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 | ||
| a0010c0019 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | ATGTC others(1252): Show |
chr15 | 80147999 | 80191349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1456 | 308 | 74 | 63 | 126 | 16 | 27 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0001t0002 | 0/0 | 1456 | 36 | 0 | 5 | 27 | 0 | 4 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0001t0003 | 0/0 | 1455 | 4 | 2 | 0 | 1 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1450): Show |
chr15 | 80147999 | 80191349 |
| a0001c0001t0004 | 0/0 | 1456 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0002t0001 | 0/0 | 1456 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0002t0003 | 0/0 | 1455 | 23 | 1 | 3 | 15 | 0 | 4 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1450): Show |
chr15 | 80147999 | 80191349 |
| a0001c0003t0001 | 0/0 | 1456 | 6 | 5 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0003t0003 | 0/0 | 1455 | 9 | 0 | 4 | 2 | 0 | 3 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1450): Show |
chr15 | 80147999 | 80191349 |
| a0001c0004t0001 | 0/0 | 1456 | 11 | 0 | 0 | 11 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0005t0001 | 0/0 | 1456 | 4 | 3 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0006t0002 | 0/0 | 1456 | 4 | 0 | 0 | 0 | 0 | 4 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0011t0001 | 0/0 | 1456 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0012t0003 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1450): Show |
chr15 | 80147999 | 80191349 |
| a0001c0014t0001 | 0/0 | 1456 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0001c0018t0003 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1450): Show |
chr15 | 80147999 | 80191349 |
| a0002c0007t0001 | 0/0 | 1456 | 4 | 4 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0003c0008t0001 | 0/0 | 1456 | 3 | 1 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0004c0009t0001 | 0/0 | 1456 | 3 | 0 | 0 | 3 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0005c0010t0001 | 0/0 | 1456 | 2 | 0 | 1 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0006c0015t0001 | 0/0 | 1456 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0007c0013t0001 | 0/0 | 1456 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0008c0016t0001 | 0/0 | 1456 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0009c0017t0001 | 0/0 | 1456 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| a0010c0019t0001 | 0/0 | 1456 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | AGTCC others(1451): Show |
chr15 | 80147999 | 80191349 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 1 | 1 | 4 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0008 | 1/0 | 6 | 0 | 2 | 0 | 2 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0006t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0006t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0006t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0006t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0011t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0012t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0014t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0001c0018t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0002c0007t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0002c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0003c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0003c0008t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0003c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0004c0009t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0004c0009t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0005c0010t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0006c0015t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0007c0013t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0008c0016t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0009c0017t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| a0010c0019t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0072 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0097 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00738 | hp1 | a0005 | c0010 | t0001 | g0005 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01346 | hp2 | a0001 | c0005 | t0001 | g0203 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0080 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01496 | hp2 | a0006 | c0015 | t0001 | g0068 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0065 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0137 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0029 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02148 | hp1 | a0001 | c0003 | t0003 | g0061 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02280 | hp2 | a0002 | c0007 | t0001 | g0232 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02451 | hp2 | a0001 | c0014 | t0001 | g0280 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02622 | hp2 | a0002 | c0007 | t0001 | g0026 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0029 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02698 | hp2 | a0001 | c0012 | t0003 | g0066 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02738 | hp2 | a0001 | c0003 | t0003 | g0067 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02818 | hp2 | a0002 | c0007 | t0001 | g0026 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0060 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0062 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03453 | hp1 | a0003 | c0008 | t0001 | g0090 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03491 | hp1 | a0001 | c0006 | t0002 | g0111 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ESN | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03540 | hp2 | a0002 | c0007 | t0001 | g0026 | AFR | GWD | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03669 | hp2 | a0001 | c0006 | t0002 | g0199 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03688 | hp2 | a0001 | c0011 | t0001 | g0146 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0086 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03831 | hp1 | a0001 | c0006 | t0002 | g0112 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03942 | hp2 | a0008 | c0016 | t0001 | g0237 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04184 | hp2 | a0001 | c0006 | t0002 | g0200 | SAS | BEB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0031 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04204 | hp2 | a0009 | c0017 | t0001 | g0094 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0017 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG04228 | hp2 | a0005 | c0010 | t0001 | g0005 | SAS | STU | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18612 | hp1 | a0004 | c0009 | t0001 | g0038 | EAS | CHB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0235 | EAS | CHB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18941 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18963 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18967 | hp1 | a0003 | c0008 | t0001 | g0150 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18983 | hp2 | a0010 | c0019 | t0001 | g0246 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18997 | hp1 | a0004 | c0009 | t0001 | g0038 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19003 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19006 | hp2 | a0001 | c0004 | t0001 | g0157 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0182 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0269 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19054 | hp2 | a0004 | c0009 | t0001 | g0103 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19077 | hp1 | a0001 | c0004 | t0001 | g0160 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19088 | hp2 | a0001 | c0003 | t0003 | g0063 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19091 | hp1 | a0003 | c0008 | t0001 | g0009 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0267 | AFR | YRI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03471 | hp1 | a0007 | c0013 | t0001 | g0271 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | USA | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA20300 | hp2 | a0001 | c0018 | t0003 | g0210 | AFR | USA | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | FAH_chr15_80147999_80191349 | FAH | chr15 | 80147999 | 80191349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:80158117 | A | G | 1 | a0002 | 4 | HG02280.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.139A>G | p.Lys47Glu | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/14 | 195/1456 | 139/1260 | 47/419 | chr15 | 80158117 | |||
| chr15:80158159 | G | T | 1 | a0004 | 3 | NA18612.hp1 NA18997.hp1 NA19054.hp2 |
missense_variant | MODERATE | c.181G>T | p.Val61Phe | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/14 | 237/1456 | 181/1260 | 61/419 | chr15 | 80158159 | |||
| chr15:80162272 | C | T | 1 | a0010 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.391C>T | p.Arg131Trp | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/14 | 447/1456 | 391/1260 | 131/419 | chr15 | 80162272 | |||
| chr15:80168108 | C | A | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.512C>A | p.Thr171Asn | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/14 | 568/1456 | 512/1260 | 171/419 | chr15 | 80168108 | |||
| chr15:80168275 | G | A | 1 | a0003 | 3 | HG03453.hp1 NA18967.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.565G>A | p.Val189Ile | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/14 | 621/1456 | 565/1260 | 189/419 | chr15 | 80168275 | |||
| chr15:80172190 | C | G | 1 | a0009 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.648C>G | p.Ile216Met | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/14 | 704/1456 | 648/1260 | 216/419 | chr15 | 80172190 | |||
| chr15:80173137 | C | T | 1 | a0008 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.830C>T | p.Pro277Leu | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/14 | 886/1456 | 830/1260 | 277/419 | chr15 | 80173137 | |||
| chr15:80180184 | C | T | 1 | a0005 | 2 | HG00738.hp1 HG04228.hp2 |
missense_variant | MODERATE | c.1021C>T | p.Arg341Trp | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/14 | 1077/1456 | 1021/1260 | 341/419 | chr15 | 80180184 | |||
| chr15:80186154 | G | A | 1 | a0006 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1205G>A | p.Arg402His | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 1261/1456 | 1205/1260 | 402/419 | chr15 | 80186154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:80158143 | C | T | 1 | a0002c0007 | 4 | HG02280.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.165C>T | p.Leu55Leu | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/14 | 221/1456 | 165/1260 | 55/419 | chr15 | 80158143 | |||
| chr15:80159812 | G | A | 1 | a0001c0011 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.249G>A | p.Val83Val | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/14 | 305/1456 | 249/1260 | 83/419 | chr15 | 80159812 | |||
| chr15:80159830 | G | C | 2 | a0001c0003 a0001c0012 |
16 | HG00733.hp2 HG01361.hp1 HG01884.hp2 others(13): Show |
synonymous_variant | LOW | c.267G>C | p.Leu89Leu | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/14 | 323/1456 | 267/1260 | 89/419 | chr15 | 80159830 | |||
| chr15:80160443 | C | T | 1 | a0001c0012 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.348C>T | p.His116His | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/14 | 404/1456 | 348/1260 | 116/419 | chr15 | 80160443 | |||
| chr15:80168079 | C | T | 1 | a0001c0018 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.483C>T | p.Gly161Gly | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/14 | 539/1456 | 483/1260 | 161/419 | chr15 | 80168079 | |||
| chr15:80173054 | A | G | 1 | a0007c0013 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.747A>G | p.Pro249Pro | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/14 | 803/1456 | 747/1260 | 249/419 | chr15 | 80173054 | |||
| chr15:80175033 | G | A | 2 | a0001c0005 a0001c0014 |
5 | HG01346.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
synonymous_variant | LOW | c.855G>A | p.Pro285Pro | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/14 | 911/1456 | 855/1260 | 285/419 | chr15 | 80175033 | |||
| chr15:80177544 | A | G | 1 | a0001c0004 | 11 | NA18941.hp2 NA18948.hp2 NA18955.hp2 others(8): Show |
synonymous_variant | LOW | c.921A>G | p.Gly307Gly | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/14 | 977/1456 | 921/1260 | 307/419 | chr15 | 80177544 | |||
| chr15:80180219 | C | T | 1 | a0001c0002 | 24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
synonymous_variant | LOW | c.1056C>T | p.Ser352Ser | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/14 | 1112/1456 | 1056/1260 | 352/419 | chr15 | 80180219 | |||
| chr15:80181077 | G | A | 1 | a0001c0014 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1098G>A | p.Ser366Ser | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/14 | 1154/1456 | 1098/1260 | 366/419 | chr15 | 80181077 | |||
| chr15:80186158 | C | T | 1 | a0001c0006 | 4 | HG03491.hp1 HG03669.hp2 HG03831.hp1 others(1): Show |
synonymous_variant | LOW | c.1209C>T | p.Ile403Ile | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 1265/1456 | 1209/1260 | 403/419 | chr15 | 80186158 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:80153012 | G | T | 1 | a0001c0001t0004 | 1 | NA19002.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/14 | 43 | chr15 | 80153012 | ||||||
| chr15:80186247 | A | C | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*38A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 38 | chr15 | 80186247 | ||||||
| chr15:80186248 | C | T | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 39 | chr15 | 80186248 | ||||||
| chr15:80186249 | C | T | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 40 | chr15 | 80186249 | ||||||
| chr15:80186250 | C | T | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 41 | chr15 | 80186250 | ||||||
| chr15:80186251 | C | G | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*42C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 42 | chr15 | 80186251 | ||||||
| chr15:80186257 | AC | A | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*51delC | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 51 | INFO_REALIGN_3_PRIME | chr15 | 80186257 | |||||
| chr15:80186297 | C | T | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0006t0002 |
41 | HG00621.hp1 HG00673.hp1 HG01123.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*88C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 88 | chr15 | 80186297 | ||||||
| chr15:80186303 | T | C | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*94T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 14/14 | 94 | chr15 | 80186303 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:80153170 | A | AG | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(57): Show |
96 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+38dupG | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153170 | ||||||
| chr15:80153171 | G | GGGAGT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0197 others(4): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+75_81+79dupGTGG others(1): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGAGTGG others(3): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0202 a0001c0005t0001g0203 |
4 | HG01167.hp2 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+70_81+79dupGTGG others(6): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGAGTGG others(8): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0204 others(4): Show |
11 | HG02451.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+65_81+79dupGTGG others(11): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGAGTGG others(13): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0209 a0001c0001t0001g0211 others(4): Show |
8 | HG01081.hp2 HG02486.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+60_81+79dupGTGG others(16): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGAGTGG others(18): Show |
4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG00140.hp2 HG01496.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+55_81+79dupGTGG others(21): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGAGTGG others(23): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0219 |
4 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+50_81+79dupGTGG others(26): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGGAGT | 10 | a0001c0001t0001g0058 a0001c0001t0001g0272 a0001c0001t0001g0273 others(7): Show |
11 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+38_81+39insGAGT others(2): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGGAGTG others(4): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
8 | HG01074.hp1 HG01106.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+38_81+39insGAGT others(7): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | G | GGGGAGTG others(9): Show |
2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.81+38_81+39insGAGT others(12): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153171 | GGGAGT | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(51): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+75_81+79delGTGG others(1): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153171 | ||||||
| chr15:80153172 | GGAGTGGA others(12): Show |
G | 23 | a0001c0001t0001g0012 a0001c0001t0001g0100 a0001c0001t0001g0110 others(20): Show |
40 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(37): Show |
intron_variant | MODIFIER | c.81+39_81+57delAGTG others(15): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153172 | ||||||
| chr15:80153473 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(52): Show |
91 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.81+338A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80153473 | |||||||
| chr15:80153518 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
6 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+383C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80153518 | |||||||
| chr15:80153625 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.81+490T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80153625 | |||||||
| chr15:80153667 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0059 |
3 | HG01069.hp1 HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.81+532C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80153667 | |||||||
| chr15:80153736 | CTT | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0100 a0001c0001t0001g0110 others(19): Show |
39 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+603_81+604delTT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 80153736 | ||||||
| chr15:80153978 | T | C | 2 | a0001c0001t0001g0114 a0001c0003t0001g0269 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.81+843T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80153978 | |||||||
| chr15:80154226 | C | A | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.81+1091C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154226 | |||||||
| chr15:80154274 | C | G | 1 | a0001c0001t0001g0047 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.81+1139C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154274 | |||||||
| chr15:80154374 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0040 others(5): Show |
14 | HG01074.hp1 HG01106.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+1239G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154374 | |||||||
| chr15:80154401 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.81+1266G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154401 | |||||||
| chr15:80154444 | T | C | 1 | a0007c0013t0001g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.81+1309T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154444 | |||||||
| chr15:80154483 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG01496.hp1 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.81+1348C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154483 | |||||||
| chr15:80154504 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+1369A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154504 | |||||||
| chr15:80154617 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+1482A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154617 | |||||||
| chr15:80154653 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+1518C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154653 | |||||||
| chr15:80154748 | A | G | 1 | a0001c0003t0003g0097 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.81+1613A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154748 | |||||||
| chr15:80154876 | C | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+1741C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154876 | |||||||
| chr15:80154898 | G | C | 2 | a0001c0005t0001g0060 a0007c0013t0001g0271 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.81+1763G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154898 | |||||||
| chr15:80154914 | G | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0034 others(13): Show |
26 | HG00099.hp1 HG01069.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+1779G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154914 | |||||||
| chr15:80154937 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
5 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+1802C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154937 | |||||||
| chr15:80154987 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+1852T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80154987 | |||||||
| chr15:80155102 | C | T | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.81+1967C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155102 | |||||||
| chr15:80155227 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.81+2092G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155227 | |||||||
| chr15:80155239 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.81+2104C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155239 | |||||||
| chr15:80155474 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0197 others(1): Show |
7 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+2339G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155474 | |||||||
| chr15:80155516 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.81+2381C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155516 | |||||||
| chr15:80155544 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0001t0001g0283 |
6 | HG02559.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+2409G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155544 | |||||||
| chr15:80155569 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
262 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(259): Show |
intron_variant | MODIFIER | c.81+2434C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155569 | |||||||
| chr15:80155576 | G | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0151 others(8): Show |
16 | HG02040.hp1 HG02129.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+2441G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155576 | |||||||
| chr15:80155606 | A | C | 1 | a0001c0001t0002g0039 | 2 | NA18952.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.82-2454A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155606 | |||||||
| chr15:80155666 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0050 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-2394G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155666 | |||||||
| chr15:80155671 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82-2389T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155671 | |||||||
| chr15:80155725 | A | T | 1 | a0001c0003t0003g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.82-2335A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155725 | |||||||
| chr15:80155793 | GC | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.82-2266delC | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155793 | |||||||
| chr15:80155859 | A | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0193 |
3 | NA18965.hp1 NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.82-2201A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155859 | |||||||
| chr15:80155892 | C | T | 7 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0005t0001g0060 others(4): Show |
7 | HG01346.hp2 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-2168C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80155892 | |||||||
| chr15:80156030 | G | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(7): Show |
18 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-2030G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156030 | |||||||
| chr15:80156134 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
301 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(298): Show |
intron_variant | MODIFIER | c.82-1926T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156134 | |||||||
| chr15:80156177 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0003g0213 |
3 | HG03516.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.82-1883C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156177 | |||||||
| chr15:80156186 | G | A | 1 | a0001c0003t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.82-1874G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156186 | |||||||
| chr15:80156192 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.82-1868T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156192 | |||||||
| chr15:80156196 | C | T | 1 | a0001c0005t0001g0203 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.82-1864C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156196 | |||||||
| chr15:80156200 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
329 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(326): Show |
intron_variant | MODIFIER | c.82-1860T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156200 | |||||||
| chr15:80156220 | G | C | 16 | a0001c0001t0001g0052 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
18 | HG00733.hp2 HG01168.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-1840G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156220 | |||||||
| chr15:80156284 | A | G | 5 | a0001c0003t0003g0065 a0001c0003t0003g0067 a0001c0003t0003g0080 others(2): Show |
5 | HG00733.hp2 HG01361.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-1776A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156284 | |||||||
| chr15:80156397 | T | C | 1 | a0008c0016t0001g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.82-1663T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156397 | |||||||
| chr15:80156543 | A | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
5 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-1517A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156543 | |||||||
| chr15:80156630 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0190 a0001c0001t0001g0191 |
6 | NA18962.hp1 NA18979.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-1430C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156630 | |||||||
| chr15:80156671 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-1389G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156671 | |||||||
| chr15:80156786 | G | C | 17 | a0001c0001t0001g0071 a0001c0002t0001g0234 a0001c0002t0003g0011 others(14): Show |
24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.82-1274G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156786 | |||||||
| chr15:80156787 | G | T | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.82-1273G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156787 | |||||||
| chr15:80156894 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.82-1166G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156894 | |||||||
| chr15:80156987 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.82-1073G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80156987 | |||||||
| chr15:80157054 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82-1006T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157054 | |||||||
| chr15:80157200 | C | T | 3 | a0001c0001t0001g0110 a0001c0006t0002g0111 a0001c0006t0002g0112 |
3 | HG02735.hp1 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.82-860C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157200 | |||||||
| chr15:80157241 | G | T | 8 | a0001c0003t0001g0064 a0001c0003t0003g0029 a0001c0003t0003g0062 others(5): Show |
9 | HG00733.hp2 HG01361.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-819G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157241 | |||||||
| chr15:80157394 | C | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0220 a0001c0002t0001g0234 others(15): Show |
25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.82-666C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157394 | |||||||
| chr15:80157615 | A | T | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.82-445A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157615 | |||||||
| chr15:80157622 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0001t0001g0283 |
6 | HG02559.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-438G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157622 | |||||||
| chr15:80157642 | C | T | 2 | a0001c0001t0001g0277 a0001c0003t0001g0269 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-418C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157642 | |||||||
| chr15:80157854 | G | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-206G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157854 | |||||||
| chr15:80157885 | G | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-175G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157885 | |||||||
| chr15:80157986 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
310 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(307): Show |
intron_variant | MODIFIER | c.82-74T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80157986 | |||||||
| chr15:80158041 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0127 a0001c0001t0001g0236 others(2): Show |
7 | HG01074.hp1 HG01106.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-19G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80158041 | |||||||
| chr15:80158047 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
241 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(238): Show |
intron_variant | MODIFIER | c.82-13G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | chr15 | 80158047 | |||||||
| chr15:80158224 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0128 |
3 | NA18964.hp1 NA18991.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.192+54G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158224 | |||||||
| chr15:80158257 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.192+87C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158257 | |||||||
| chr15:80158270 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.192+100G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158270 | |||||||
| chr15:80158279 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.192+109G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158279 | |||||||
| chr15:80158348 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+178T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158348 | |||||||
| chr15:80158369 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.192+199C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158369 | |||||||
| chr15:80158382 | G | A | 24 | a0001c0001t0001g0110 a0001c0001t0002g0004 a0001c0001t0002g0010 others(21): Show |
39 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.192+212G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158382 | |||||||
| chr15:80158479 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.192+309G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158479 | |||||||
| chr15:80158618 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.192+448A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158618 | |||||||
| chr15:80158940 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192+770T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80158940 | |||||||
| chr15:80159080 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0034 others(8): Show |
21 | HG00099.hp1 HG01069.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-676A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159080 | |||||||
| chr15:80159227 | GA | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
271 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(268): Show |
intron_variant | MODIFIER | c.193-518delA | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 80159227 | ||||||
| chr15:80159228 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.193-528A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159228 | |||||||
| chr15:80159260 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-496G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159260 | |||||||
| chr15:80159265 | A | G | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.193-491A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159265 | |||||||
| chr15:80159287 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.193-469T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159287 | |||||||
| chr15:80159343 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
92 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.193-413G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159343 | |||||||
| chr15:80159422 | ACT | A | 16 | a0001c0001t0001g0071 a0001c0002t0003g0011 a0001c0002t0003g0017 others(13): Show |
23 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-331_193-330del others(2): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 80159422 | ||||||
| chr15:80159437 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193-319G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159437 | |||||||
| chr15:80159461 | G | A | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193-295G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159461 | |||||||
| chr15:80159581 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.193-175T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159581 | |||||||
| chr15:80159671 | C | T | 15 | a0001c0003t0001g0064 a0001c0003t0001g0118 a0001c0003t0001g0121 others(12): Show |
16 | HG00733.hp2 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.193-85C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159671 | |||||||
| chr15:80159733 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
281 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(278): Show |
intron_variant | MODIFIER | c.193-23T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 2/13 | chr15 | 80159733 | |||||||
| chr15:80159926 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
283 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(280): Show |
intron_variant | MODIFIER | c.314+49G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80159926 | |||||||
| chr15:80159932 | G | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.314+55G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80159932 | |||||||
| chr15:80160013 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.314+136C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160013 | |||||||
| chr15:80160101 | C | G | 19 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0220 others(16): Show |
28 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.314+224C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160101 | |||||||
| chr15:80160117 | C | G | 1 | a0001c0003t0003g0067 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+240C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160117 | |||||||
| chr15:80160174 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.315-236G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160174 | |||||||
| chr15:80160194 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.315-216G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160194 | |||||||
| chr15:80160229 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(5): Show |
16 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.315-181G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 3/13 | chr15 | 80160229 | |||||||
| chr15:80160502 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364+43G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160502 | |||||||
| chr15:80160544 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
200 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.364+85T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160544 | |||||||
| chr15:80160601 | G | T | 10 | a0001c0003t0001g0064 a0001c0003t0003g0029 a0001c0003t0003g0061 others(7): Show |
11 | HG00733.hp2 HG01361.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+142G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160601 | |||||||
| chr15:80160705 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.364+246G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160705 | |||||||
| chr15:80160741 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.364+282C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160741 | |||||||
| chr15:80160744 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+285A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160744 | |||||||
| chr15:80160839 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.364+380G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160839 | |||||||
| chr15:80160953 | G | A | 26 | a0001c0001t0001g0110 a0001c0001t0001g0196 a0001c0001t0002g0004 others(23): Show |
41 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(38): Show |
intron_variant | MODIFIER | c.364+494G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80160953 | |||||||
| chr15:80161095 | C | A | 1 | a0006c0015t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.364+636C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161095 | |||||||
| chr15:80161172 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364+713C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161172 | |||||||
| chr15:80161271 | G | GT | 14 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0188 others(11): Show |
15 | HG01109.hp2 HG01346.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.364+827dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr15 | 80161271 | ||||||
| chr15:80161271 | GT | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0041 others(9): Show |
21 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.364+827delT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr15 | 80161271 | ||||||
| chr15:80161329 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.364+870C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161329 | |||||||
| chr15:80161388 | G | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(394): Show |
intron_variant | MODIFIER | c.365-858G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161388 | |||||||
| chr15:80161414 | TG | T | 26 | a0001c0001t0001g0110 a0001c0001t0001g0196 a0001c0001t0002g0004 others(23): Show |
41 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(38): Show |
intron_variant | MODIFIER | c.365-831delG | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161414 | |||||||
| chr15:80161491 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.365-755A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161491 | |||||||
| chr15:80161572 | T | C | 59 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0041 others(56): Show |
84 | HG00673.hp1 HG00733.hp2 HG01123.hp1 others(81): Show |
intron_variant | MODIFIER | c.365-674T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161572 | |||||||
| chr15:80161600 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
285 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(282): Show |
intron_variant | MODIFIER | c.365-646A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161600 | |||||||
| chr15:80161629 | C | T | 18 | a0001c0001t0001g0277 a0001c0001t0001g0284 a0001c0003t0001g0064 others(15): Show |
19 | HG00733.hp2 HG01361.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.365-617C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161629 | |||||||
| chr15:80161845 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
204 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.365-401A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80161845 | |||||||
| chr15:80162137 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.365-109A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80162137 | |||||||
| chr15:80162164 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.365-82C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 4/13 | chr15 | 80162164 | |||||||
| chr15:80162365 | G | A | 26 | a0001c0001t0001g0110 a0001c0001t0001g0196 a0001c0001t0002g0004 others(23): Show |
41 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(38): Show |
intron_variant | MODIFIER | c.455+29G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162365 | |||||||
| chr15:80162400 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455+64T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162400 | |||||||
| chr15:80162403 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
201 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.455+67T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162403 | |||||||
| chr15:80162463 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.455+127G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162463 | |||||||
| chr15:80162488 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.455+152G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162488 | |||||||
| chr15:80162551 | A | T | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.455+215A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162551 | |||||||
| chr15:80162817 | C | A | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.455+481C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162817 | |||||||
| chr15:80162873 | A | C | 1 | a0001c0003t0003g0065 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.455+537A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162873 | |||||||
| chr15:80162892 | A | G | 5 | a0001c0003t0003g0065 a0001c0003t0003g0067 a0001c0003t0003g0080 others(2): Show |
5 | HG00733.hp2 HG01361.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.455+556A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162892 | |||||||
| chr15:80162933 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.455+597C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80162933 | |||||||
| chr15:80163174 | C | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0273 |
3 | HG02572.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.455+838C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163174 | |||||||
| chr15:80163179 | A | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
283 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(280): Show |
intron_variant | MODIFIER | c.455+843A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163179 | |||||||
| chr15:80163485 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
201 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.455+1149C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163485 | |||||||
| chr15:80163554 | A | T | 3 | a0001c0014t0001g0280 a0002c0007t0001g0026 a0002c0007t0001g0232 |
5 | HG02280.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.455+1218A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163554 | |||||||
| chr15:80163788 | G | A | 26 | a0001c0001t0001g0110 a0001c0001t0001g0196 a0001c0001t0002g0004 others(23): Show |
41 | HG00673.hp1 HG01123.hp1 HG01928.hp1 others(38): Show |
intron_variant | MODIFIER | c.455+1452G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163788 | |||||||
| chr15:80163994 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.455+1658G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80163994 | |||||||
| chr15:80164067 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.455+1731G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164067 | |||||||
| chr15:80164145 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455+1809G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164145 | |||||||
| chr15:80164529 | A | AAC | 21 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0220 others(18): Show |
30 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.455+2210_455+2211d others(4): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80164529 | ||||||
| chr15:80164529 | A | AACAC | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0041 others(10): Show |
22 | HG01255.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.455+2208_455+2211d others(6): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80164529 | ||||||
| chr15:80164555 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.455+2219C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164555 | |||||||
| chr15:80164599 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.455+2263C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164599 | |||||||
| chr15:80164670 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.455+2334G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164670 | |||||||
| chr15:80164824 | C | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0034 others(18): Show |
31 | HG00099.hp1 HG01069.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.455+2488C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164824 | |||||||
| chr15:80164836 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.455+2500A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164836 | |||||||
| chr15:80164894 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.455+2558G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164894 | |||||||
| chr15:80164901 | C | T | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.455+2565C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80164901 | |||||||
| chr15:80165251 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.456-2801A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165251 | |||||||
| chr15:80165271 | G | C | 1 | a0001c0001t0001g0052 | 2 | HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.456-2781G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165271 | |||||||
| chr15:80165280 | C | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.456-2772C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165280 | |||||||
| chr15:80165386 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.456-2666G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165386 | |||||||
| chr15:80165453 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.456-2599G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165453 | |||||||
| chr15:80165514 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.456-2538C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165514 | |||||||
| chr15:80165515 | G | A | 5 | a0001c0002t0003g0069 a0001c0002t0003g0123 a0001c0002t0003g0125 others(2): Show |
5 | HG02004.hp2 HG03209.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.456-2537G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165515 | |||||||
| chr15:80165527 | C | CA | 13 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(10): Show |
15 | HG01496.hp1 HG02055.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.456-2507dupA | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80165527 | ||||||
| chr15:80165563 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.456-2489C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165563 | |||||||
| chr15:80165564 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(11): Show |
22 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.456-2488G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165564 | |||||||
| chr15:80165567 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456-2485C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165567 | |||||||
| chr15:80165618 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.456-2434C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165618 | |||||||
| chr15:80165811 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0001g0202 others(13): Show |
32 | HG00558.hp1 HG00609.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.456-2241G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165811 | |||||||
| chr15:80165911 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0007c0013t0001g0271 |
3 | HG02615.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.456-2141C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80165911 | |||||||
| chr15:80166163 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.456-1889C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166163 | |||||||
| chr15:80166206 | C | A | 13 | a0001c0003t0001g0118 a0001c0003t0001g0121 a0001c0003t0001g0122 others(10): Show |
14 | HG00733.hp2 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.456-1846C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166206 | |||||||
| chr15:80166287 | C | A | 20 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0220 others(17): Show |
29 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.456-1765C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166287 | |||||||
| chr15:80166481 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.456-1571T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166481 | |||||||
| chr15:80166560 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.456-1492T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166560 | |||||||
| chr15:80166567 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.456-1485A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166567 | |||||||
| chr15:80166619 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
94 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.456-1433C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166619 | |||||||
| chr15:80166635 | C | CT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
176 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.456-1398dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80166635 | ||||||
| chr15:80166635 | C | CTT | 16 | a0001c0001t0001g0027 a0001c0001t0001g0089 a0001c0001t0001g0096 others(13): Show |
18 | HG01074.hp1 HG01106.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.456-1399_456-1398d others(4): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80166635 | ||||||
| chr15:80166640 | T | C | 19 | a0001c0001t0001g0085 a0001c0001t0001g0188 a0001c0001t0001g0277 others(16): Show |
20 | HG00733.hp2 HG01361.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.456-1412T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166640 | |||||||
| chr15:80166705 | C | T | 1 | a0001c0002t0003g0075 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.456-1347C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166705 | |||||||
| chr15:80166722 | C | T | 4 | a0001c0005t0001g0060 a0001c0005t0001g0192 a0001c0005t0001g0203 others(1): Show |
4 | HG01346.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-1330C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166722 | |||||||
| chr15:80166791 | C | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 |
3 | HG02145.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.456-1261C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166791 | |||||||
| chr15:80166915 | C | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(399): Show |
intron_variant | MODIFIER | c.456-1137C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166915 | |||||||
| chr15:80166930 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.456-1122C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80166930 | |||||||
| chr15:80167057 | G | GT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
150 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.456-985dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80167057 | ||||||
| chr15:80167083 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.456-969G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167083 | |||||||
| chr15:80167093 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(58): Show |
99 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.456-959G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167093 | |||||||
| chr15:80167367 | G | A | 1 | a0001c0002t0003g0030 | 2 | NA19011.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.456-685G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167367 | |||||||
| chr15:80167374 | TCTC | T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0176 others(17): Show |
29 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.456-672_456-670del others(3): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80167374 | ||||||
| chr15:80167414 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.456-638T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167414 | |||||||
| chr15:80167465 | C | T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0220 others(17): Show |
29 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.456-587C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167465 | |||||||
| chr15:80167530 | CT | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
300 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.456-503delT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80167530 | ||||||
| chr15:80167530 | CTT | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0115 others(13): Show |
19 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.456-504_456-503del others(2): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80167530 | ||||||
| chr15:80167530 | CTTT | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0050 others(3): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.456-505_456-503del others(3): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 80167530 | ||||||
| chr15:80167554 | T | C | 1 | a0003c0008t0001g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.456-498T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167554 | |||||||
| chr15:80167641 | T | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.456-411T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167641 | |||||||
| chr15:80167785 | G | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(10): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.456-267G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167785 | |||||||
| chr15:80167867 | C | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.456-185C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80167867 | |||||||
| chr15:80168032 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
7 | HG02080.hp2 NA18943.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.456-20C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 5/13 | chr15 | 80168032 | |||||||
| chr15:80168182 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
331 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.553+33A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/13 | chr15 | 80168182 | |||||||
| chr15:80168219 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.554-45C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/13 | chr15 | 80168219 | |||||||
| chr15:80168234 | G | GT | 23 | a0001c0001t0001g0095 a0001c0001t0001g0134 a0001c0001t0001g0173 others(20): Show |
23 | HG00140.hp1 HG01261.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.554-16dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 80168234 | ||||||
| chr15:80168234 | G | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.554-30G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 6/13 | chr15 | 80168234 | |||||||
| chr15:80168365 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.606+49A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168365 | |||||||
| chr15:80168368 | A | G | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.606+52A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168368 | |||||||
| chr15:80168574 | T | C | 1 | a0001c0001t0003g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.606+258T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168574 | |||||||
| chr15:80168587 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(101): Show |
152 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(149): Show |
intron_variant | MODIFIER | c.606+271G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168587 | |||||||
| chr15:80168714 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.606+398A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168714 | |||||||
| chr15:80168778 | T | A | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+462T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168778 | |||||||
| chr15:80168937 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.606+621A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168937 | |||||||
| chr15:80168961 | C | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+645C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168961 | |||||||
| chr15:80168968 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.606+652G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80168968 | |||||||
| chr15:80169013 | A | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+697A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169013 | |||||||
| chr15:80169104 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0131 |
3 | HG00558.hp2 NA18952.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.606+788C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169104 | |||||||
| chr15:80169202 | G | A | 2 | a0001c0001t0002g0053 a0007c0013t0001g0271 |
3 | HG03471.hp1 NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.606+886G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169202 | |||||||
| chr15:80169338 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0195 |
2 | NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.606+1022G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169338 | |||||||
| chr15:80169382 | CAAAACAA others(7): Show |
C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1077_606+1090d others(16): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 80169382 | ||||||
| chr15:80169457 | A | G | 1 | a0006c0015t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.606+1141A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169457 | |||||||
| chr15:80169574 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0284 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.606+1258C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169574 | |||||||
| chr15:80169591 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.606+1275T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169591 | |||||||
| chr15:80169659 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.606+1343G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169659 | |||||||
| chr15:80169670 | A | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1354A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169670 | |||||||
| chr15:80169690 | T | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1374T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169690 | |||||||
| chr15:80169755 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.606+1439G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169755 | |||||||
| chr15:80169760 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.606+1444C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169760 | |||||||
| chr15:80169775 | C | G | 1 | a0001c0001t0002g0104 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.606+1459C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169775 | |||||||
| chr15:80169823 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.606+1507G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169823 | |||||||
| chr15:80169943 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.606+1627C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80169943 | |||||||
| chr15:80170000 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.606+1684A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170000 | |||||||
| chr15:80170174 | G | A | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.606+1858G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170174 | |||||||
| chr15:80170204 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0254 |
2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.606+1888G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170204 | |||||||
| chr15:80170263 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0059 |
3 | HG01069.hp1 HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.607-1886T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170263 | |||||||
| chr15:80170299 | A | G | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.607-1850A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170299 | |||||||
| chr15:80170369 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(140): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.607-1780G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170369 | |||||||
| chr15:80170379 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.607-1770T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170379 | |||||||
| chr15:80170527 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.607-1622C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170527 | |||||||
| chr15:80170620 | A | G | 1 | a0001c0001t0001g0019 | 3 | HG01070.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.607-1529A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170620 | |||||||
| chr15:80170662 | A | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.607-1487A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170662 | |||||||
| chr15:80170731 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.607-1418G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170731 | |||||||
| chr15:80170734 | C | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.607-1415C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170734 | |||||||
| chr15:80170766 | T | G | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.607-1383T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170766 | |||||||
| chr15:80170789 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0059 |
3 | HG01069.hp1 HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.607-1360G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170789 | |||||||
| chr15:80170903 | C | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.607-1246C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170903 | |||||||
| chr15:80170957 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.607-1192G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170957 | |||||||
| chr15:80170987 | C | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.607-1162C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170987 | |||||||
| chr15:80170988 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.607-1161G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80170988 | |||||||
| chr15:80171127 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.607-1022G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171127 | |||||||
| chr15:80171156 | C | G | 1 | a0001c0001t0001g0020 | 3 | HG01069.hp2 HG01071.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.607-993C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171156 | |||||||
| chr15:80171235 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0188 a0001c0001t0001g0277 others(2): Show |
5 | HG01496.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-914C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171235 | |||||||
| chr15:80171244 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.607-905T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171244 | |||||||
| chr15:80171245 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.607-904T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171245 | |||||||
| chr15:80171340 | T | TGCCTACA others(3): Show |
67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
96 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.607-808_607-807ins others(10): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 80171340 | ||||||
| chr15:80171342 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
96 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.607-807T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171342 | |||||||
| chr15:80171344 | G | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
96 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.607-805G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171344 | |||||||
| chr15:80171346 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
96 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.607-803G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171346 | |||||||
| chr15:80171410 | T | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.607-739T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171410 | |||||||
| chr15:80171444 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.607-705T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171444 | |||||||
| chr15:80171541 | G | T | 1 | a0001c0001t0002g0240 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.607-608G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171541 | |||||||
| chr15:80171635 | T | G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0208 others(7): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-514T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171635 | |||||||
| chr15:80171811 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0003g0213 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-338C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171811 | |||||||
| chr15:80171921 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.607-228G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171921 | |||||||
| chr15:80171943 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.607-206C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171943 | |||||||
| chr15:80171973 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0047 others(3): Show |
14 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-176T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 7/13 | chr15 | 80171973 | |||||||
| chr15:80172309 | A | G | 7 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 others(4): Show |
7 | HG01346.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.706+61A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172309 | |||||||
| chr15:80172327 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
96 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.706+79A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172327 | |||||||
| chr15:80172443 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.706+195A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172443 | |||||||
| chr15:80172450 | C | CAT | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(107): Show |
159 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.706+202_706+203ins others(2): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172450 | |||||||
| chr15:80172521 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 |
3 | HG02145.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.706+273A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172521 | |||||||
| chr15:80172541 | C | T | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.706+293C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172541 | |||||||
| chr15:80172542 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(74): Show |
110 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.706+294C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172542 | |||||||
| chr15:80172587 | A | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.706+339A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172587 | |||||||
| chr15:80172715 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707-299C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172715 | |||||||
| chr15:80172769 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.707-245G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172769 | |||||||
| chr15:80172892 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.707-122G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172892 | |||||||
| chr15:80172906 | GA | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.707-107delA | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172906 | |||||||
| chr15:80172951 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0282 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.707-63G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172951 | |||||||
| chr15:80172958 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0247 others(12): Show |
33 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.707-56G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 8/13 | chr15 | 80172958 | |||||||
| chr15:80173241 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0282 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.837+97G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173241 | |||||||
| chr15:80173261 | C | T | 1 | a0001c0003t0003g0063 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.837+117C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173261 | |||||||
| chr15:80173421 | G | A | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.837+277G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173421 | |||||||
| chr15:80173438 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.837+294G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173438 | |||||||
| chr15:80173578 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.837+434G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173578 | |||||||
| chr15:80173779 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.837+635C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173779 | |||||||
| chr15:80173834 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.837+690C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173834 | |||||||
| chr15:80173918 | C | T | 5 | a0001c0001t0001g0220 a0001c0003t0001g0118 a0001c0003t0001g0121 others(2): Show |
5 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+774C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173918 | |||||||
| chr15:80173922 | G | C | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.837+778G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173922 | |||||||
| chr15:80173951 | G | A | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.837+807G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173951 | |||||||
| chr15:80173972 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.837+828C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173972 | |||||||
| chr15:80173982 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.837+838A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173982 | |||||||
| chr15:80173996 | C | G | 2 | a0001c0004t0001g0249 a0001c0004t0001g0251 |
2 | NA18941.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.837+852C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80173996 | |||||||
| chr15:80174315 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.838-701A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174315 | |||||||
| chr15:80174316 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
5 | HG01168.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-700C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174316 | |||||||
| chr15:80174507 | T | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
5 | HG01168.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-509T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174507 | |||||||
| chr15:80174572 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.838-444C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174572 | |||||||
| chr15:80174633 | C | T | 3 | a0001c0004t0001g0157 a0001c0004t0001g0159 a0001c0004t0001g0160 |
3 | NA18999.hp1 NA19006.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.838-383C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174633 | |||||||
| chr15:80174721 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.838-295C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174721 | |||||||
| chr15:80174820 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.838-196A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174820 | |||||||
| chr15:80174824 | AC | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0141 others(1): Show |
7 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-189delC | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr15 | 80174824 | ||||||
| chr15:80174837 | TC | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.838-173delC | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr15 | 80174837 | ||||||
| chr15:80174940 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.838-76T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174940 | |||||||
| chr15:80174966 | G | A | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.838-50G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 9/13 | chr15 | 80174966 | |||||||
| chr15:80175105 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.913+14G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175105 | |||||||
| chr15:80175206 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.913+115G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175206 | |||||||
| chr15:80175247 | G | C | 18 | a0001c0001t0001g0071 a0001c0002t0001g0234 a0001c0002t0003g0011 others(15): Show |
25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.913+156G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175247 | |||||||
| chr15:80175284 | G | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.913+193G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175284 | |||||||
| chr15:80175533 | T | A | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.913+442T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175533 | |||||||
| chr15:80175552 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.913+461C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175552 | |||||||
| chr15:80175622 | A | G | 9 | a0001c0003t0003g0029 a0001c0003t0003g0061 a0001c0003t0003g0062 others(6): Show |
10 | HG00733.hp2 HG01361.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.913+531A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175622 | |||||||
| chr15:80175680 | G | A | 2 | a0001c0001t0002g0101 a0007c0013t0001g0271 |
2 | HG02056.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.913+589G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175680 | |||||||
| chr15:80175798 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.913+707C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175798 | |||||||
| chr15:80175830 | A | G | 3 | a0001c0002t0003g0017 a0001c0002t0003g0075 a0001c0002t0003g0086 |
5 | HG01934.hp2 HG01943.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+739A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175830 | |||||||
| chr15:80175858 | GA | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
5 | HG01168.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+768delA | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175858 | |||||||
| chr15:80175905 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0050 others(4): Show |
12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+814A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80175905 | |||||||
| chr15:80176051 | C | G | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.913+960C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176051 | |||||||
| chr15:80176054 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(52): Show |
95 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.913+963C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176054 | |||||||
| chr15:80176106 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.913+1015C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176106 | |||||||
| chr15:80176239 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+1148C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176239 | |||||||
| chr15:80176244 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.913+1153A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176244 | |||||||
| chr15:80176262 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0007c0013t0001g0271 |
3 | HG02615.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.913+1171C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176262 | |||||||
| chr15:80176270 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.913+1179C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176270 | |||||||
| chr15:80176295 | C | T | 1 | a0001c0001t0002g0010 | 5 | HG01123.hp1 HG01928.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+1204C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176295 | |||||||
| chr15:80176354 | T | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-1183T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176354 | |||||||
| chr15:80176430 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0142 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.914-1107G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176430 | |||||||
| chr15:80176481 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0283 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.914-1056A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176481 | |||||||
| chr15:80176540 | C | T | 1 | a0001c0001t0001g0057 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.914-997C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176540 | |||||||
| chr15:80176597 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-940C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176597 | |||||||
| chr15:80176622 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.914-915G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176622 | |||||||
| chr15:80176629 | G | T | 5 | a0001c0001t0001g0220 a0001c0003t0001g0118 a0001c0003t0001g0121 others(2): Show |
5 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-908G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176629 | |||||||
| chr15:80176683 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-854C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176683 | |||||||
| chr15:80176684 | G | A | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.914-853G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176684 | |||||||
| chr15:80176692 | A | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-845A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176692 | |||||||
| chr15:80176752 | C | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.914-785C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176752 | |||||||
| chr15:80176756 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0188 a0001c0001t0001g0277 others(2): Show |
5 | HG01496.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-781C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80176756 | |||||||
| chr15:80177092 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.914-445A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80177092 | |||||||
| chr15:80177221 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-316T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80177221 | |||||||
| chr15:80177232 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.914-305C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80177232 | |||||||
| chr15:80177240 | A | G | 9 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0208 others(6): Show |
13 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.914-297A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 10/13 | chr15 | 80177240 | |||||||
| chr15:80177648 | C | T | 4 | a0001c0005t0001g0060 a0001c0005t0001g0192 a0001c0005t0001g0203 others(1): Show |
4 | HG01346.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+65C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80177648 | |||||||
| chr15:80177698 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
138 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.960+115G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80177698 | |||||||
| chr15:80178025 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.960+442C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178025 | |||||||
| chr15:80178060 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.960+477C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178060 | |||||||
| chr15:80178084 | C | T | 14 | a0001c0001t0001g0220 a0001c0003t0001g0118 a0001c0003t0001g0121 others(11): Show |
15 | HG00733.hp2 HG01361.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.960+501C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178084 | |||||||
| chr15:80178115 | G | A | 24 | a0001c0001t0001g0085 a0001c0001t0001g0115 a0001c0001t0001g0188 others(21): Show |
25 | HG00733.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.960+532G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178115 | |||||||
| chr15:80178117 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.960+534T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178117 | |||||||
| chr15:80178153 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(94): Show |
160 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.960+570T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178153 | |||||||
| chr15:80178176 | C | G | 1 | a0001c0002t0003g0123 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.960+593C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178176 | |||||||
| chr15:80178177 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
138 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.960+594G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178177 | |||||||
| chr15:80178213 | TA | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(82): Show |
141 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.960+637delA | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr15 | 80178213 | ||||||
| chr15:80178236 | G | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.960+653G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178236 | |||||||
| chr15:80178301 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.960+718A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178301 | |||||||
| chr15:80178327 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.960+744G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178327 | |||||||
| chr15:80178332 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
5 | HG02165.hp1 NA18940.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+749G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178332 | |||||||
| chr15:80178492 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
342 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(339): Show |
intron_variant | MODIFIER | c.960+909C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178492 | |||||||
| chr15:80178587 | A | AT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.960+1019dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr15 | 80178587 | ||||||
| chr15:80178587 | A | ATT | 23 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0056 others(20): Show |
33 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.960+1018_960+1019d others(4): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr15 | 80178587 | ||||||
| chr15:80178587 | AT | A | 17 | a0001c0001t0001g0100 a0001c0002t0001g0234 a0001c0002t0003g0011 others(14): Show |
24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.960+1019delT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr15 | 80178587 | ||||||
| chr15:80178591 | T | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.960+1008T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178591 | |||||||
| chr15:80178684 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.960+1101T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178684 | |||||||
| chr15:80178809 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(52): Show |
95 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.960+1226C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178809 | |||||||
| chr15:80178848 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0206 |
5 | HG02451.hp1 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1265A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178848 | |||||||
| chr15:80178877 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0093 a0001c0001t0001g0095 |
4 | NA18999.hp2 NA19003.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-1247T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178877 | |||||||
| chr15:80178883 | C | T | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-1241C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178883 | |||||||
| chr15:80178925 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.961-1199C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178925 | |||||||
| chr15:80178964 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
159 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.961-1160C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178964 | |||||||
| chr15:80178989 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0283 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.961-1135C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80178989 | |||||||
| chr15:80179085 | G | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(107): Show |
158 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.961-1039G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179085 | |||||||
| chr15:80179117 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.961-1007C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179117 | |||||||
| chr15:80179120 | G | T | 1 | a0001c0002t0003g0073 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.961-1004G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179120 | |||||||
| chr15:80179121 | T | A | 1 | a0001c0002t0003g0073 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.961-1003T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179121 | |||||||
| chr15:80179122 | A | G | 1 | a0001c0002t0003g0073 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.961-1002A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179122 | |||||||
| chr15:80179149 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.961-975A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179149 | |||||||
| chr15:80179164 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
157 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(154): Show |
intron_variant | MODIFIER | c.961-960C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179164 | |||||||
| chr15:80179176 | C | T | 30 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0041 others(27): Show |
40 | HG00733.hp2 HG01255.hp1 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.961-948C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179176 | |||||||
| chr15:80179333 | C | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0197 others(1): Show |
7 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-791C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179333 | |||||||
| chr15:80179438 | A | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-686A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179438 | |||||||
| chr15:80179447 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.961-677G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179447 | |||||||
| chr15:80179481 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0284 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.961-643G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179481 | |||||||
| chr15:80179518 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.961-606G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179518 | |||||||
| chr15:80179534 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0003g0213 a0001c0001t0003g0270 |
3 | HG01891.hp2 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.961-590C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179534 | |||||||
| chr15:80179600 | C | T | 23 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 others(20): Show |
30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.961-524C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179600 | |||||||
| chr15:80179670 | C | T | 8 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0220 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-454C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179670 | |||||||
| chr15:80179704 | C | T | 4 | a0001c0005t0001g0060 a0001c0005t0001g0192 a0001c0005t0001g0203 others(1): Show |
4 | HG01346.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-420C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179704 | |||||||
| chr15:80179864 | G | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0007c0013t0001g0271 |
3 | HG02615.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.961-260G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179864 | |||||||
| chr15:80179901 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(399): Show |
intron_variant | MODIFIER | c.961-223T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80179901 | |||||||
| chr15:80180045 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG03927.hp1 NA18961.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.961-79G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80180045 | |||||||
| chr15:80180071 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.961-53A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80180071 | |||||||
| chr15:80180089 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.961-35C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 11/13 | chr15 | 80180089 | |||||||
| chr15:80180476 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0007c0013t0001g0271 |
3 | HG02615.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1062+251C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180476 | |||||||
| chr15:80180579 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0007c0013t0001g0271 |
3 | HG02615.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1062+354G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180579 | |||||||
| chr15:80180601 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1062+376G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180601 | |||||||
| chr15:80180665 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1063-377G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180665 | |||||||
| chr15:80180915 | C | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 |
3 | HG02145.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1063-127C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180915 | |||||||
| chr15:80180946 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0284 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1063-96C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180946 | |||||||
| chr15:80180992 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1063-50A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 12/13 | chr15 | 80180992 | |||||||
| chr15:80181163 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(10): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1180+4A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181163 | |||||||
| chr15:80181206 | T | C | 1 | a0001c0003t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1180+47T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181206 | |||||||
| chr15:80181228 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1180+69G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181228 | |||||||
| chr15:80181242 | A | G | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1180+83A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181242 | |||||||
| chr15:80181272 | T | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(34): Show |
52 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1180+113T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181272 | |||||||
| chr15:80181320 | A | G | 9 | a0001c0003t0003g0029 a0001c0003t0003g0061 a0001c0003t0003g0062 others(6): Show |
10 | HG00733.hp2 HG01361.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1180+161A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181320 | |||||||
| chr15:80181525 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(52): Show |
95 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1180+366C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181525 | |||||||
| chr15:80181731 | T | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1180+572T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181731 | |||||||
| chr15:80181744 | T | G | 5 | a0001c0001t0001g0220 a0001c0003t0001g0118 a0001c0003t0001g0121 others(2): Show |
5 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+585T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181744 | |||||||
| chr15:80181856 | CTG | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1180+700_1180+701d others(4): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 80181856 | ||||||
| chr15:80181881 | G | A | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1180+722G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181881 | |||||||
| chr15:80181892 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
154 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(151): Show |
intron_variant | MODIFIER | c.1180+733C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181892 | |||||||
| chr15:80181895 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1180+736G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181895 | |||||||
| chr15:80181904 | G | A | 1 | a0001c0002t0003g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1180+745G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181904 | |||||||
| chr15:80181919 | C | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1180+760C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80181919 | |||||||
| chr15:80182011 | T | A | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1180+852T>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182011 | |||||||
| chr15:80182044 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | NA18999.hp2 NA19003.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+885C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182044 | |||||||
| chr15:80182049 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1180+890T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182049 | |||||||
| chr15:80182077 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1180+918G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182077 | |||||||
| chr15:80182079 | G | A | 10 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0208 others(7): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+920G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182079 | |||||||
| chr15:80182104 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1180+945G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182104 | |||||||
| chr15:80182171 | T | C | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1180+1012T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182171 | |||||||
| chr15:80182177 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0178 |
2 | NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1180+1018C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182177 | |||||||
| chr15:80182370 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1180+1211A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182370 | |||||||
| chr15:80182372 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1180+1213G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182372 | |||||||
| chr15:80182381 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1180+1222A>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182381 | |||||||
| chr15:80182532 | C | G | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1180+1373C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182532 | |||||||
| chr15:80182553 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(10): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1180+1394T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182553 | |||||||
| chr15:80182609 | C | T | 1 | a0003c0008t0001g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180+1450C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182609 | |||||||
| chr15:80182678 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(10): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1180+1519A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182678 | |||||||
| chr15:80182684 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1180+1525G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182684 | |||||||
| chr15:80182699 | T | C | 23 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0001g0272 others(20): Show |
30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1180+1540T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182699 | |||||||
| chr15:80182929 | C | T | 1 | a0008c0016t0001g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1180+1770C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80182929 | |||||||
| chr15:80183261 | G | T | 2 | a0001c0001t0003g0213 a0001c0001t0003g0270 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1180+2102G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183261 | |||||||
| chr15:80183336 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(49): Show |
92 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1180+2177G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183336 | |||||||
| chr15:80183389 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1180+2230G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183389 | |||||||
| chr15:80183424 | T | C | 21 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(18): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1180+2265T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183424 | |||||||
| chr15:80183441 | T | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1180+2282T>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183441 | |||||||
| chr15:80183459 | A | G | 1 | a0001c0014t0001g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1180+2300A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183459 | |||||||
| chr15:80183714 | C | T | 1 | a0009c0017t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1181-2416C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183714 | |||||||
| chr15:80183897 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1181-2233A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80183897 | |||||||
| chr15:80184069 | G | A | 1 | a0001c0018t0003g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1181-2061G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184069 | |||||||
| chr15:80184096 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1181-2034G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184096 | |||||||
| chr15:80184159 | C | T | 3 | a0001c0002t0003g0123 a0001c0002t0003g0125 a0001c0002t0003g0137 |
3 | HG02004.hp2 NA18975.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1181-1971C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184159 | |||||||
| chr15:80184233 | A | G | 20 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(17): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-1897A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184233 | |||||||
| chr15:80184237 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1181-1893G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184237 | |||||||
| chr15:80184298 | C | A | 1 | a0001c0001t0002g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1181-1832C>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184298 | |||||||
| chr15:80184416 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(49): Show |
92 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1181-1714C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184416 | |||||||
| chr15:80184451 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.1181-1679A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184451 | |||||||
| chr15:80184510 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1181-1620C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184510 | |||||||
| chr15:80184574 | C | CT | 20 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(17): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-1547dupT | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 80184574 | ||||||
| chr15:80184577 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | NA19012.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1181-1553T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184577 | |||||||
| chr15:80184613 | T | C | 20 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(17): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-1517T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184613 | |||||||
| chr15:80184732 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0204 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-1398A>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184732 | |||||||
| chr15:80184781 | C | T | 19 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(16): Show |
25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1181-1349C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184781 | |||||||
| chr15:80184795 | T | C | 1 | a0006c0015t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181-1335T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184795 | |||||||
| chr15:80184893 | C | G | 1 | a0001c0003t0001g0122 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1181-1237C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184893 | |||||||
| chr15:80184897 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1181-1233C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184897 | |||||||
| chr15:80184909 | C | G | 1 | a0001c0001t0001g0259 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1181-1221C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184909 | |||||||
| chr15:80184927 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1181-1203C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80184927 | |||||||
| chr15:80185015 | C | T | 17 | a0001c0002t0001g0234 a0001c0002t0003g0011 a0001c0002t0003g0017 others(14): Show |
24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1181-1115C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185015 | |||||||
| chr15:80185018 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1181-1112C>G | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185018 | |||||||
| chr15:80185167 | G | C | 5 | a0001c0001t0001g0220 a0001c0003t0001g0118 a0001c0003t0001g0121 others(2): Show |
5 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-963G>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185167 | |||||||
| chr15:80185185 | T | C | 1 | a0001c0006t0002g0111 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1181-945T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185185 | |||||||
| chr15:80185229 | G | A | 20 | a0001c0001t0003g0213 a0001c0001t0003g0270 a0001c0002t0001g0234 others(17): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-901G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185229 | |||||||
| chr15:80185391 | G | T | 9 | a0001c0002t0003g0011 a0001c0002t0003g0030 a0001c0002t0003g0070 others(6): Show |
13 | HG00408.hp1 HG00621.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181-739G>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185391 | |||||||
| chr15:80185484 | T | C | 1 | a0006c0015t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181-646T>C | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185484 | |||||||
| chr15:80185755 | C | T | 27 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0128 others(24): Show |
41 | HG00621.hp1 HG00673.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1181-375C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185755 | |||||||
| chr15:80185839 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0169 a0001c0001t0001g0178 others(2): Show |
8 | NA18962.hp1 NA18979.hp1 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-291C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185839 | |||||||
| chr15:80185858 | A | T | 4 | a0001c0002t0003g0011 a0001c0002t0003g0070 a0001c0002t0003g0073 others(1): Show |
7 | HG00408.hp1 NA18954.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-272A>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185858 | |||||||
| chr15:80185888 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1181-242G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185888 | |||||||
| chr15:80185895 | C | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
72 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1181-235C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185895 | |||||||
| chr15:80185920 | G | A | 30 | a0001c0001t0001g0119 a0001c0001t0003g0183 a0001c0001t0003g0213 others(27): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1181-210G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185920 | |||||||
| chr15:80185926 | G | A | 30 | a0001c0001t0001g0119 a0001c0001t0003g0183 a0001c0001t0003g0213 others(27): Show |
38 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1181-204G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80185926 | |||||||
| chr15:80186032 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0050 others(4): Show |
12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1181-98C>T | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80186032 | |||||||
| chr15:80186082 | G | A | 1 | a0007c0013t0001g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181-48G>A | FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 13/13 | chr15 | 80186082 |