Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130540 |
| ensemblid | ENSG00000155749.13 |
| hgncid | 14439 |
| symbol | FLACC1 |
| name | flagellum associated containing coiled-coil domains 1 |
| refseq_nuc | NM_001127391.3 |
| refseq_prot | NP_001120863.1 |
| ensembl_nuc | ENST00000392257.8 |
| ensembl_prot | ENSP00000376086.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 201288271 |
| end | 201357345 |
| strand | - |
| ver | v1.2 |
| region | chr2:201288271-201357345 |
| region5000 | chr2:201283271-201362345 |
| regionname0 | FLACC1_chr2_201288271_201357345 |
| regionname5000 | FLACC1_chr2_201283271_201362345 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 422 | 255 | 68 | 33 | 119 | 5 | 29 | 93 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| a0002 | 1/0 | 422 | 110 | 19 | 35 | 41 | 5 | 9 | 29 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| a0003 | 0/0 | 422 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| a0004 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| a0005 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| a0006 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | MYPNP others(417): Show |
chr2 | 201283271 | 201362345 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1266 | 251 | 67 | 32 | 118 | 5 | 28 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0001c0005 | 0/0 | 1266 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0001c0007 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0001c0009 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0001c0012 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0002c0002 | 1/0 | 1266 | 97 | 15 | 30 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0002c0003 | 0/0 | 1266 | 12 | 3 | 5 | 1 | 3 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0002c0011 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0003c0004 | 0/0 | 1266 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0004c0006 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0005c0010 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 | ||
| a0006c0008 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | ATGTA others(1261): Show |
chr2 | 201283271 | 201362345 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2064 | 97 | 4 | 25 | 54 | 4 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0003 | 0/0 | 2064 | 59 | 8 | 0 | 42 | 0 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0004 | 0/0 | 2064 | 36 | 32 | 4 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0005 | 0/0 | 2064 | 14 | 0 | 0 | 13 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0006 | 0/0 | 2064 | 22 | 11 | 2 | 4 | 0 | 5 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0007 | 0/0 | 2064 | 12 | 7 | 1 | 0 | 0 | 4 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0008 | 0/0 | 2064 | 6 | 2 | 0 | 4 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0009 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0011 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0012 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0001t0013 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0005t0006 | 0/0 | 2064 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0007t0001 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0009t0001 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0001c0012t0001 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0002t0002 | 1/0 | 2064 | 89 | 12 | 25 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0002t0003 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0002t0004 | 0/0 | 2064 | 4 | 2 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0002t0005 | 0/0 | 2064 | 3 | 0 | 3 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0003t0005 | 0/0 | 2064 | 11 | 3 | 5 | 1 | 2 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0003t0010 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0002c0011t0005 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0003c0004t0005 | 0/0 | 2064 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0004c0006t0003 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0005c0010t0004 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| a0006c0008t0007 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | CAACT others(2059): Show |
chr2 | 201283271 | 201362345 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0008g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0012g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0001t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0005t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0001c0012t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0002 | 1/0 | 6 | 5 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0003t0010g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0002c0011t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0003c0004t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0003c0004t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0004c0006t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0005c0010t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| a0006c0008t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00140 | hp2 | a0002 | c0003 | t0005 | g0222 | EUR | GBR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0164 | EUR | FIN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00738 | hp1 | a0002 | c0003 | t0005 | g0223 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0206 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01069 | hp1 | a0002 | c0003 | t0005 | g0226 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01074 | hp2 | a0002 | c0003 | t0005 | g0219 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01109 | hp1 | a0001 | c0005 | t0006 | g0039 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01167 | hp1 | a0002 | c0002 | t0005 | g0158 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0217 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01169 | hp2 | a0002 | c0002 | t0005 | g0159 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01192 | hp1 | a0002 | c0003 | t0005 | g0227 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01261 | hp1 | a0002 | c0003 | t0005 | g0225 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0187 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0124 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0314 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01517 | hp1 | a0002 | c0003 | t0005 | g0224 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01884 | hp2 | a0004 | c0006 | t0003 | g0304 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02027 | hp1 | a0002 | c0003 | t0005 | g0221 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0171 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0307 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02622 | hp1 | a0002 | c0003 | t0005 | g0215 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02630 | hp1 | a0003 | c0004 | t0005 | g0312 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0313 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02717 | hp2 | a0005 | c0010 | t0004 | g0156 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02738 | hp2 | a0001 | c0007 | t0001 | g0125 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02818 | hp2 | a0003 | c0004 | t0005 | g0311 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02895 | hp1 | a0001 | c0009 | t0001 | g0050 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0210 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03225 | hp1 | a0002 | c0003 | t0005 | g0214 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0120 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0241 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0115 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0119 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0149 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0041 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0196 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19001 | hp1 | a0001 | c0012 | t0001 | g0146 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19030 | hp2 | a0006 | c0008 | t0007 | g0075 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19043 | hp1 | a0002 | c0011 | t0005 | g0205 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0139 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0172 | EUR | TSI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20752 | hp2 | a0002 | c0003 | t0010 | g0218 | EUR | TSI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | GIH | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0110 | SAS | GIH | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0157 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| HG06807 | hp2 | a0002 | c0002 | t0004 | g0211 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA21309 | hp1 | a0002 | c0003 | t0005 | g0220 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0315 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0133 | REF | REF | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0002 | REF | REF | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201299292 | C | G | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.888G>C | p.Leu296Phe | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/15 | 1299/2064 | 888/1269 | 296/422 | chr2 | 201299292 | |||
| chr2:201330765 | G | T | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.593C>A | p.Ala198Glu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/15 | 1004/2064 | 593/1269 | 198/422 | chr2 | 201330765 | |||
| chr2:201346672 | C | G | 1 | a0005 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.238G>C | p.Val80Leu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/15 | 649/2064 | 238/1269 | 80/422 | chr2 | 201346672 | |||
| chr2:201348272 | C | G | 1 | a0003 | 2 | HG02630.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.216G>C | p.Glu72Asp | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/15 | 627/2064 | 216/1269 | 72/422 | chr2 | 201348272 | |||
| chr2:201350769 | C | G | 4 | a0001 a0003 a0004 others(1): Show |
258 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
missense_variant | MODERATE | c.127G>C | p.Val43Leu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/15 | 538/2064 | 127/1269 | 43/422 | chr2 | 201350769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201289477 | C | T | 4 | a0001c0009 a0002c0003 a0002c0011 others(1): Show |
16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
synonymous_variant | LOW | c.1122G>A | p.Thr374Thr | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/15 | 1533/2064 | 1122/1269 | 374/422 | chr2 | 201289477 | |||
| chr2:201309203 | C | T | 1 | a0001c0007 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.723G>A | p.Ala241Ala | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/15 | 1134/2064 | 723/1269 | 241/422 | chr2 | 201309203 | |||
| chr2:201346661 | C | T | 1 | a0002c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.249G>A | p.Val83Val | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/15 | 660/2064 | 249/1269 | 83/422 | chr2 | 201346661 | |||
| chr2:201350761 | A | G | 1 | a0001c0005 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.135T>C | p.Ala45Ala | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/15 | 546/2064 | 135/1269 | 45/422 | chr2 | 201350761 | |||
| chr2:201351381 | G | A | 1 | a0001c0012 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.24C>T | p.Tyr8Tyr | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/15 | 435/2064 | 24/1269 | 8/422 | chr2 | 201351381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201288355 | T | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(15): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*300A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 300 | chr2 | 201288355 | ||||||
| chr2:201288429 | G | A | 1 | a0001c0001t0009 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 226 | chr2 | 201288429 | ||||||
| chr2:201288502 | C | A | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*153G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 153 | chr2 | 201288502 | ||||||
| chr2:201288529 | A | C | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(9): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*126T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 126 | chr2 | 201288529 | ||||||
| chr2:201288653 | G | A | 1 | a0002c0003t0010 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 2 | chr2 | 201288653 | ||||||
| chr2:201357198 | C | T | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(7): Show |
142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-264G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5794 | chr2 | 201357198 | ||||||
| chr2:201357208 | T | C | 1 | a0001c0001t0011 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-274A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5804 | chr2 | 201357208 | ||||||
| chr2:201357243 | T | C | 1 | a0001c0001t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-309A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5839 | chr2 | 201357243 | ||||||
| chr2:201357337 | C | A | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5933 | chr2 | 201357337 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201288873 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143-92C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288873 | |||||||
| chr2:201288961 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(242): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.1143-180G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288961 | |||||||
| chr2:201288974 | A | G | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1143-193T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288974 | |||||||
| chr2:201289066 | C | T | 10 | a0002c0002t0002g0021 a0002c0002t0002g0024 a0002c0002t0002g0025 others(7): Show |
14 | HG00639.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1143-285G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289066 | |||||||
| chr2:201289123 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(103): Show |
117 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1142+334C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289123 | |||||||
| chr2:201289157 | A | AC | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(103): Show |
117 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1142+299dupG | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289157 | |||||||
| chr2:201289197 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(242): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.1142+260T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289197 | |||||||
| chr2:201289247 | GGGAGAAG others(4): Show |
G | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1142+199_1142+209d others(13): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289247 | |||||||
| chr2:201289674 | C | G | 47 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(44): Show |
55 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.1032+22G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 13/14 | chr2 | 201289674 | |||||||
| chr2:201289810 | G | A | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.943-25C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289810 | |||||||
| chr2:201289875 | G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-90C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289875 | |||||||
| chr2:201289960 | C | A | 2 | a0002c0003t0005g0220 a0002c0003t0005g0223 |
2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.943-175G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289960 | |||||||
| chr2:201290027 | G | A | 5 | a0002c0002t0002g0026 a0002c0002t0002g0155 a0002c0002t0002g0177 others(2): Show |
6 | HG00639.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-242C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290027 | |||||||
| chr2:201290182 | T | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0092 others(10): Show |
16 | HG00323.hp2 HG00639.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.943-397A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290182 | |||||||
| chr2:201290218 | T | C | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-433A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290218 | |||||||
| chr2:201290425 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00323.hp2 HG01243.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.943-640G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290425 | |||||||
| chr2:201290510 | G | A | 1 | a0001c0001t0008g0045 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.943-725C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290510 | |||||||
| chr2:201290603 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.943-818G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290603 | |||||||
| chr2:201290711 | T | C | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.943-926A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290711 | |||||||
| chr2:201290716 | C | T | 7 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-931G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290716 | |||||||
| chr2:201290743 | C | T | 1 | a0001c0001t0003g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.943-958G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290743 | |||||||
| chr2:201290744 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.943-959C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290744 | |||||||
| chr2:201290839 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.943-1054G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290839 | |||||||
| chr2:201290855 | T | C | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943-1070A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290855 | |||||||
| chr2:201290863 | G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-1078C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290863 | |||||||
| chr2:201290918 | G | A | 1 | a0001c0001t0004g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.943-1133C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290918 | |||||||
| chr2:201290923 | G | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0097 |
2 | NA19062.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.943-1138C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290923 | |||||||
| chr2:201290959 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.943-1174C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290959 | |||||||
| chr2:201290963 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.943-1178A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290963 | |||||||
| chr2:201290973 | G | A | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943-1188C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290973 | |||||||
| chr2:201291078 | C | T | 1 | a0002c0002t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.943-1293G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291078 | |||||||
| chr2:201291098 | G | A | 14 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(11): Show |
15 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.943-1313C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291098 | |||||||
| chr2:201291331 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(194): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.943-1546A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291331 | |||||||
| chr2:201291331 | T | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-1546A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291331 | |||||||
| chr2:201291502 | T | C | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-1717A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291502 | |||||||
| chr2:201291601 | T | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.943-1816A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291601 | |||||||
| chr2:201291649 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.943-1864C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291649 | |||||||
| chr2:201291672 | T | A | 76 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(73): Show |
86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.943-1887A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291672 | |||||||
| chr2:201291688 | C | T | 1 | a0002c0002t0002g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.943-1903G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291688 | |||||||
| chr2:201291727 | C | T | 4 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 others(1): Show |
4 | HG02300.hp2 NA18939.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-1942G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291727 | |||||||
| chr2:201291822 | A | G | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.943-2037T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291822 | |||||||
| chr2:201292069 | CAGGG | C | 19 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(16): Show |
26 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.943-2288_943-2285d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292069 | |||||||
| chr2:201292134 | G | T | 1 | a0002c0002t0002g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.943-2349C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292134 | |||||||
| chr2:201292144 | G | A | 1 | a0002c0002t0002g0181 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.943-2359C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292144 | |||||||
| chr2:201292202 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.943-2417C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292202 | |||||||
| chr2:201292281 | C | G | 1 | a0002c0002t0002g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.943-2496G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292281 | |||||||
| chr2:201292283 | C | T | 1 | a0002c0002t0002g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.943-2498G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292283 | |||||||
| chr2:201292367 | A | G | 1 | a0001c0001t0001g0006 | 3 | HG00140.hp1 HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.943-2582T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292367 | |||||||
| chr2:201292525 | A | G | 1 | a0002c0002t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.943-2740T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292525 | |||||||
| chr2:201292546 | A | G | 1 | a0001c0001t0005g0280 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.943-2761T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292546 | |||||||
| chr2:201292579 | T | C | 1 | a0001c0001t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.943-2794A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292579 | |||||||
| chr2:201292800 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0140 |
2 | NA18962.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.943-3015T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292800 | |||||||
| chr2:201293001 | G | A | 1 | a0002c0003t0010g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.943-3216C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293001 | |||||||
| chr2:201293108 | C | T | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.943-3323G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293108 | |||||||
| chr2:201293133 | G | T | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-3348C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293133 | |||||||
| chr2:201293206 | G | C | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-3421C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293206 | |||||||
| chr2:201293238 | C | T | 9 | a0001c0001t0001g0040 a0002c0002t0002g0022 a0002c0002t0002g0166 others(6): Show |
10 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-3453G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293238 | |||||||
| chr2:201293279 | A | T | 1 | a0001c0001t0006g0114 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.943-3494T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293279 | |||||||
| chr2:201293309 | C | T | 1 | a0001c0001t0003g0028 | 2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.943-3524G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293309 | |||||||
| chr2:201293320 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.943-3535C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293320 | |||||||
| chr2:201293373 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.943-3588G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293373 | |||||||
| chr2:201293390 | A | C | 2 | a0001c0001t0007g0115 a0001c0001t0007g0149 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.943-3605T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293390 | |||||||
| chr2:201293404 | A | T | 13 | a0002c0003t0005g0214 a0002c0003t0005g0215 a0002c0003t0005g0219 others(10): Show |
13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.943-3619T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293404 | |||||||
| chr2:201293602 | A | G | 5 | a0001c0001t0003g0010 a0001c0001t0003g0030 a0001c0001t0003g0252 others(2): Show |
8 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-3817T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293602 | |||||||
| chr2:201293617 | G | C | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-3832C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293617 | |||||||
| chr2:201293625 | A | G | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-3840T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293625 | |||||||
| chr2:201293816 | G | A | 75 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(72): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.943-4031C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293816 | |||||||
| chr2:201293817 | C | CA | 121 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(118): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.943-4033dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293817 | |||||||
| chr2:201293827 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(194): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.943-4042G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293827 | |||||||
| chr2:201293881 | G | A | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.943-4096C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293881 | |||||||
| chr2:201293909 | C | G | 92 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(89): Show |
102 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.943-4124G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293909 | |||||||
| chr2:201293953 | A | C | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.943-4168T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293953 | |||||||
| chr2:201294048 | A | C | 3 | a0001c0001t0003g0310 a0001c0001t0011g0313 a0002c0002t0003g0157 |
3 | HG02109.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.943-4263T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294048 | |||||||
| chr2:201294291 | A | C | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-4506T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294291 | |||||||
| chr2:201294328 | C | A | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.943-4543G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294328 | |||||||
| chr2:201294403 | C | T | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.943-4618G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294403 | |||||||
| chr2:201294473 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.943-4688G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294473 | |||||||
| chr2:201294474 | G | A | 1 | a0002c0002t0002g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.943-4689C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294474 | |||||||
| chr2:201294568 | C | T | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.942+4670G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294568 | |||||||
| chr2:201294618 | G | T | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.942+4620C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294618 | |||||||
| chr2:201294678 | G | T | 5 | a0001c0001t0003g0236 a0001c0001t0003g0246 a0001c0001t0003g0266 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+4560C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294678 | |||||||
| chr2:201294734 | C | T | 67 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(64): Show |
76 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.942+4504G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294734 | |||||||
| chr2:201294775 | A | G | 1 | a0001c0001t0007g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.942+4463T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294775 | |||||||
| chr2:201294803 | T | C | 1 | a0002c0002t0002g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.942+4435A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294803 | |||||||
| chr2:201295085 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.942+4153C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295085 | |||||||
| chr2:201295376 | T | C | 1 | a0001c0001t0007g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.942+3862A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295376 | |||||||
| chr2:201295393 | A | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(66): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.942+3845T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295393 | |||||||
| chr2:201295595 | G | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+3643C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295595 | |||||||
| chr2:201295655 | G | A | 3 | a0001c0001t0006g0109 a0001c0001t0006g0110 a0001c0001t0006g0112 |
3 | HG01168.hp2 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.942+3583C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295655 | |||||||
| chr2:201295933 | C | A | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.942+3305G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295933 | |||||||
| chr2:201295945 | A | G | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.942+3293T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295945 | |||||||
| chr2:201295948 | C | CA | 4 | a0001c0001t0001g0065 a0001c0001t0001g0091 a0001c0001t0001g0153 others(1): Show |
4 | HG03017.hp2 HG03453.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+3289dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295948 | |||||||
| chr2:201296039 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.942+3199G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296039 | |||||||
| chr2:201296225 | C | T | 87 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0053 others(84): Show |
97 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.942+3013G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296225 | |||||||
| chr2:201296259 | A | C | 1 | a0001c0001t0005g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.942+2979T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296259 | |||||||
| chr2:201296269 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.942+2969G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296269 | |||||||
| chr2:201296310 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(222): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.942+2928A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296310 | |||||||
| chr2:201296331 | C | T | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+2907G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296331 | |||||||
| chr2:201296344 | G | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.942+2894C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296344 | |||||||
| chr2:201296420 | C | A | 1 | a0001c0001t0004g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.942+2818G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296420 | |||||||
| chr2:201296500 | C | T | 7 | a0001c0001t0007g0069 a0001c0001t0007g0070 a0001c0001t0007g0071 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+2738G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296500 | |||||||
| chr2:201296564 | A | G | 93 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(90): Show |
103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.942+2674T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296564 | |||||||
| chr2:201296663 | A | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0140 |
2 | NA18962.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.942+2575T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296663 | |||||||
| chr2:201296913 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.942+2325C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296913 | |||||||
| chr2:201297170 | T | C | 1 | a0001c0001t0005g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.942+2068A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297170 | |||||||
| chr2:201297309 | G | C | 1 | a0001c0007t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.942+1929C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297309 | |||||||
| chr2:201297310 | T | TGTACTGA others(47): Show |
1 | a0001c0007t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.942+1927_942+1928i others(56): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297310 | |||||||
| chr2:201297419 | T | TG | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.942+1818dupC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297419 | |||||||
| chr2:201297497 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+1741C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297497 | |||||||
| chr2:201297615 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.942+1623G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297615 | |||||||
| chr2:201297679 | TGAGGTGT others(6): Show |
T | 1 | a0001c0001t0003g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.942+1546_942+1558d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297679 | |||||||
| chr2:201297683 | G | C | 66 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(63): Show |
75 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.942+1555C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297683 | |||||||
| chr2:201297852 | C | T | 4 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0151 others(1): Show |
4 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+1386G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297852 | |||||||
| chr2:201297934 | G | A | 67 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(64): Show |
76 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.942+1304C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297934 | |||||||
| chr2:201298070 | G | A | 2 | a0002c0002t0002g0186 a0002c0002t0002g0193 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.942+1168C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298070 | |||||||
| chr2:201298088 | A | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(222): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.942+1150T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298088 | |||||||
| chr2:201298182 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.942+1056C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298182 | |||||||
| chr2:201298320 | T | C | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.942+918A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298320 | |||||||
| chr2:201298379 | C | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+859G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298379 | |||||||
| chr2:201298421 | C | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.942+817G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298421 | |||||||
| chr2:201298510 | C | T | 1 | a0001c0001t0004g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.942+728G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298510 | |||||||
| chr2:201298542 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.942+696A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298542 | |||||||
| chr2:201298744 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.942+494G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298744 | |||||||
| chr2:201298760 | G | A | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.942+478C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298760 | |||||||
| chr2:201299127 | T | G | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.942+111A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201299127 | |||||||
| chr2:201299703 | G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-403C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299703 | |||||||
| chr2:201299828 | C | T | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.880-528G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299828 | |||||||
| chr2:201299832 | G | A | 1 | a0001c0001t0003g0261 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.880-532C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299832 | |||||||
| chr2:201299932 | G | A | 1 | a0002c0002t0002g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.880-632C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299932 | |||||||
| chr2:201300082 | C | G | 10 | a0002c0003t0005g0219 a0002c0003t0005g0220 a0002c0003t0005g0221 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-782G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300082 | |||||||
| chr2:201300103 | C | T | 1 | a0002c0002t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.880-803G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300103 | |||||||
| chr2:201300114 | A | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.880-814T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300114 | |||||||
| chr2:201300129 | G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-829C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300129 | |||||||
| chr2:201300194 | C | T | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.880-894G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300194 | |||||||
| chr2:201300241 | C | T | 1 | a0001c0001t0004g0005 | 4 | HG02886.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-941G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300241 | |||||||
| chr2:201300303 | C | T | 1 | a0001c0001t0006g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.880-1003G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300303 | |||||||
| chr2:201300315 | T | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-1015A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300315 | |||||||
| chr2:201300358 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.880-1058G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300358 | |||||||
| chr2:201300483 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.880-1183A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300483 | |||||||
| chr2:201300524 | A | C | 2 | a0001c0001t0004g0298 a0001c0001t0004g0302 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.880-1224T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300524 | |||||||
| chr2:201300784 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.880-1484C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300784 | |||||||
| chr2:201300960 | A | G | 1 | a0001c0007t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880-1660T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300960 | |||||||
| chr2:201301021 | C | T | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.880-1721G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301021 | |||||||
| chr2:201301207 | T | C | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1907A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301207 | |||||||
| chr2:201301228 | GT | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0080 others(2): Show |
6 | HG02523.hp1 NA18945.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1929delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301228 | |||||||
| chr2:201301692 | T | A | 3 | a0002c0002t0002g0207 a0002c0002t0002g0208 a0002c0002t0002g0209 |
3 | HG00642.hp2 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.880-2392A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301692 | |||||||
| chr2:201301744 | T | C | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-2444A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301744 | |||||||
| chr2:201301868 | T | C | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-2568A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301868 | |||||||
| chr2:201301869 | A | T | 72 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(69): Show |
81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.880-2569T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301869 | |||||||
| chr2:201302208 | G | T | 1 | a0002c0002t0002g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.880-2908C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302208 | |||||||
| chr2:201302232 | T | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0053 others(18): Show |
22 | HG00544.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.880-2932A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302232 | |||||||
| chr2:201302280 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.880-2980G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302280 | |||||||
| chr2:201302360 | C | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.880-3060G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302360 | |||||||
| chr2:201302383 | A | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.880-3083T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302383 | |||||||
| chr2:201302487 | C | A | 7 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-3187G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302487 | |||||||
| chr2:201302810 | A | C | 2 | a0001c0001t0001g0134 a0002c0002t0002g0021 |
3 | HG01256.hp2 HG01258.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.880-3510T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302810 | |||||||
| chr2:201302928 | G | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.880-3628C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302928 | |||||||
| chr2:201303013 | T | G | 1 | a0002c0002t0002g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.880-3713A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303013 | |||||||
| chr2:201303046 | C | CA | 17 | a0001c0001t0013g0315 a0001c0009t0001g0050 a0002c0003t0005g0214 others(14): Show |
17 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.880-3747dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303046 | |||||||
| chr2:201303054 | A | G | 1 | a0001c0001t0003g0031 | 2 | NA18986.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.880-3754T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303054 | |||||||
| chr2:201303108 | C | CA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(223): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.880-3809dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303108 | |||||||
| chr2:201303127 | C | G | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880-3827G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303127 | |||||||
| chr2:201303177 | C | T | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-3877G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303177 | |||||||
| chr2:201303317 | C | G | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-4017G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303317 | |||||||
| chr2:201303361 | C | A | 3 | a0001c0009t0001g0050 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.880-4061G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303361 | |||||||
| chr2:201303373 | T | A | 1 | a0001c0001t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.880-4073A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303373 | |||||||
| chr2:201303473 | G | A | 1 | a0001c0001t0004g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.879+4046C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303473 | |||||||
| chr2:201303492 | A | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+4027T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303492 | |||||||
| chr2:201303519 | C | T | 1 | a0001c0001t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.879+4000G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303519 | |||||||
| chr2:201303562 | T | C | 1 | a0001c0001t0005g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.879+3957A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303562 | |||||||
| chr2:201303924 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+3595C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303924 | |||||||
| chr2:201303929 | T | A | 1 | a0001c0001t0003g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.879+3590A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303929 | |||||||
| chr2:201303941 | G | A | 1 | a0001c0001t0006g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.879+3578C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303941 | |||||||
| chr2:201303982 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.879+3537C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303982 | |||||||
| chr2:201303983 | G | C | 2 | a0001c0001t0007g0115 a0001c0001t0007g0149 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.879+3536C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303983 | |||||||
| chr2:201304026 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.879+3493A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304026 | |||||||
| chr2:201304041 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.879+3478T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304041 | |||||||
| chr2:201304060 | G | C | 94 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(91): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.879+3459C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304060 | |||||||
| chr2:201304270 | A | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+3249T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304270 | |||||||
| chr2:201304369 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.879+3150A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304369 | |||||||
| chr2:201304384 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.879+3135C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304384 | |||||||
| chr2:201304409 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(223): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.879+3110A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304409 | |||||||
| chr2:201304432 | G | A | 68 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(65): Show |
77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.879+3087C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304432 | |||||||
| chr2:201304708 | C | T | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+2811G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304708 | |||||||
| chr2:201304760 | G | A | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2759C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304760 | |||||||
| chr2:201304761 | C | G | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2758G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304761 | |||||||
| chr2:201304899 | G | A | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | NA18939.hp1 NA18974.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.879+2620C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304899 | |||||||
| chr2:201304997 | C | T | 18 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(15): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.879+2522G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304997 | |||||||
| chr2:201305068 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.879+2451G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305068 | |||||||
| chr2:201305217 | G | T | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+2302C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305217 | |||||||
| chr2:201305270 | G | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
21 | HG02056.hp2 HG02071.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.879+2249C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305270 | |||||||
| chr2:201305390 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.879+2129A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305390 | |||||||
| chr2:201305411 | G | C | 1 | a0002c0002t0002g0179 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.879+2108C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305411 | |||||||
| chr2:201305526 | C | T | 2 | a0002c0002t0005g0158 a0002c0002t0005g0159 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.879+1993G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305526 | |||||||
| chr2:201305655 | T | C | 5 | a0001c0001t0006g0123 a0001c0001t0006g0126 a0001c0001t0006g0127 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1864A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305655 | |||||||
| chr2:201305684 | A | C | 5 | a0001c0001t0006g0123 a0001c0001t0006g0126 a0001c0001t0006g0127 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1835T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305684 | |||||||
| chr2:201305691 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.879+1828G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305691 | |||||||
| chr2:201305692 | C | G | 5 | a0001c0001t0006g0123 a0001c0001t0006g0126 a0001c0001t0006g0127 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1827G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305692 | |||||||
| chr2:201305694 | T | A | 5 | a0001c0001t0006g0123 a0001c0001t0006g0126 a0001c0001t0006g0127 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1825A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305694 | |||||||
| chr2:201305866 | T | C | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+1653A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305866 | |||||||
| chr2:201305932 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.879+1587A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305932 | |||||||
| chr2:201305935 | G | T | 77 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(74): Show |
87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.879+1584C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305935 | |||||||
| chr2:201306089 | A | T | 3 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0308 |
6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+1430T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306089 | |||||||
| chr2:201306099 | T | TA | 20 | a0001c0001t0003g0249 a0001c0001t0004g0004 a0001c0001t0004g0005 others(17): Show |
27 | HG01167.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1419dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306099 | |||||||
| chr2:201306099 | TA | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(110): Show |
124 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.879+1419delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306099 | |||||||
| chr2:201306249 | G | A | 1 | a0001c0001t0009g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.879+1270C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306249 | |||||||
| chr2:201306269 | T | A | 1 | a0001c0001t0007g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.879+1250A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306269 | |||||||
| chr2:201306373 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.879+1146T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306373 | |||||||
| chr2:201306679 | T | C | 12 | a0002c0003t0005g0214 a0002c0003t0005g0215 a0002c0003t0005g0219 others(9): Show |
12 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.879+840A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306679 | |||||||
| chr2:201306786 | C | CA | 26 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(23): Show |
27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+732dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306786 | |||||||
| chr2:201306850 | C | G | 46 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(43): Show |
54 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.879+669G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306850 | |||||||
| chr2:201307127 | T | C | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.879+392A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201307127 | |||||||
| chr2:201307468 | G | A | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+51C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201307468 | |||||||
| chr2:201307677 | A | G | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.776-55T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201307677 | |||||||
| chr2:201307972 | A | G | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.776-350T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201307972 | |||||||
| chr2:201308409 | C | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.775+742G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201308409 | |||||||
| chr2:201308415 | T | C | 3 | a0001c0009t0001g0050 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.775+736A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201308415 | |||||||
| chr2:201309089 | C | A | 18 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(15): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.775+62G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201309089 | |||||||
| chr2:201309100 | G | A | 2 | a0001c0001t0003g0310 a0004c0006t0003g0304 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.775+51C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201309100 | |||||||
| chr2:201309794 | C | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-544G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309794 | |||||||
| chr2:201309855 | C | T | 1 | a0001c0001t0005g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.676-605G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309855 | |||||||
| chr2:201309905 | C | CA | 12 | a0001c0001t0004g0285 a0001c0001t0004g0305 a0001c0001t0004g0307 others(9): Show |
14 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.676-656dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | |||||||
| chr2:201309905 | C | CAAAAA | 7 | a0001c0001t0013g0315 a0002c0003t0005g0219 a0002c0003t0005g0220 others(4): Show |
7 | HG00140.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-660_676-656dup others(5): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | |||||||
| chr2:201309905 | C | CAAAAAA | 8 | a0001c0009t0001g0050 a0002c0003t0005g0215 a0002c0003t0005g0221 others(5): Show |
8 | HG01069.hp1 HG01192.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-661_676-656dup others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | |||||||
| chr2:201309922 | A | G | 1 | a0001c0001t0003g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.676-672T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309922 | |||||||
| chr2:201309925 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-676_676-675ins others(28): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(19): Show |
3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0116 |
3 | HG01978.hp2 HG03471.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.676-676_676-675ins others(26): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(18): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0090 others(1): Show |
4 | HG02071.hp1 HG02129.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(25): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(17): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0072 others(12): Show |
19 | HG00738.hp2 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(24): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(16): Show |
39 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0040 others(36): Show |
40 | HG00673.hp2 HG01243.hp2 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(23): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(15): Show |
27 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
28 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAAAAA others(14): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0038 others(3): Show |
9 | HG00140.hp1 HG01106.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(21): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AAAAG | 6 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(3): Show |
7 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AG | 3 | a0001c0001t0001g0086 a0002c0002t0005g0158 a0002c0002t0005g0159 |
3 | HG01123.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.676-676_676-675ins others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | AGAAG | 64 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(61): Show |
73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201309925 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0003g0231 a0001c0001t0003g0264 |
3 | HG00621.hp1 HG00621.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.676-675T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | |||||||
| chr2:201310246 | T | TC | 96 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0003g0010 others(93): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-997_676-996ins others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310246 | |||||||
| chr2:201310248 | T | A | 96 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0003g0010 others(93): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-998A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310248 | |||||||
| chr2:201310249 | C | T | 96 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0003g0010 others(93): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-999G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310249 | |||||||
| chr2:201310250 | C | G | 96 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0003g0010 others(93): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-1000G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310250 | |||||||
| chr2:201310251 | C | A | 96 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0003g0010 others(93): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-1001G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310251 | |||||||
| chr2:201310258 | T | A | 1 | a0002c0002t0002g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.676-1008A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310258 | |||||||
| chr2:201310267 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(99): Show |
113 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.676-1017C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310267 | |||||||
| chr2:201310406 | C | T | 1 | a0001c0001t0006g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.676-1156G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310406 | |||||||
| chr2:201310473 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.676-1223T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310473 | |||||||
| chr2:201310920 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.676-1670G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310920 | |||||||
| chr2:201310933 | C | T | 60 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(57): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.676-1683G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310933 | |||||||
| chr2:201311046 | T | C | 94 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(91): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.676-1796A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311046 | |||||||
| chr2:201311158 | T | TA | 20 | a0001c0001t0003g0249 a0001c0001t0003g0310 a0001c0001t0004g0288 others(17): Show |
20 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.676-1909dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311158 | |||||||
| chr2:201311158 | TA | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0099 a0001c0001t0001g0106 others(4): Show |
7 | HG00323.hp2 HG00673.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-1909delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311158 | |||||||
| chr2:201311179 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-1929C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311179 | |||||||
| chr2:201311301 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.676-2051A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311301 | |||||||
| chr2:201311315 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.676-2065A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311315 | |||||||
| chr2:201311571 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.676-2321T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311571 | |||||||
| chr2:201311672 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-2422C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311672 | |||||||
| chr2:201311688 | G | A | 2 | a0002c0003t0005g0221 a0002c0003t0010g0218 |
2 | HG02027.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.676-2438C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311688 | |||||||
| chr2:201311700 | C | CA | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(139): Show |
155 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.676-2451dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311700 | |||||||
| chr2:201311700 | C | CAA | 85 | a0001c0001t0001g0099 a0001c0001t0003g0010 a0001c0001t0003g0028 others(82): Show |
101 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.676-2452_676-2451d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311700 | |||||||
| chr2:201311804 | A | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-2554T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311804 | |||||||
| chr2:201311927 | C | A | 1 | a0001c0001t0003g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.676-2677G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311927 | |||||||
| chr2:201311934 | A | G | 13 | a0002c0003t0005g0214 a0002c0003t0005g0215 a0002c0003t0005g0219 others(10): Show |
13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-2684T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311934 | |||||||
| chr2:201312314 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.676-3064G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312314 | |||||||
| chr2:201312734 | CG | C | 19 | a0001c0001t0001g0099 a0001c0001t0004g0004 a0001c0001t0004g0005 others(16): Show |
26 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.676-3485delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312734 | |||||||
| chr2:201312816 | G | A | 24 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(21): Show |
25 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.676-3566C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312816 | |||||||
| chr2:201312863 | C | T | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-3613G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312863 | |||||||
| chr2:201312915 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.676-3665C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312915 | |||||||
| chr2:201313038 | G | T | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-3788C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313038 | |||||||
| chr2:201313059 | G | C | 1 | a0002c0002t0002g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.676-3809C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313059 | |||||||
| chr2:201313149 | C | A | 2 | a0002c0002t0002g0186 a0002c0002t0002g0193 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.676-3899G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313149 | |||||||
| chr2:201313149 | C | G | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.676-3899G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313149 | |||||||
| chr2:201313235 | A | C | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.676-3985T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313235 | |||||||
| chr2:201313363 | C | G | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676-4113G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313363 | |||||||
| chr2:201313366 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-4116C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313366 | |||||||
| chr2:201313407 | C | T | 18 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(15): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.676-4157G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313407 | |||||||
| chr2:201313408 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.676-4158C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313408 | |||||||
| chr2:201313514 | T | C | 5 | a0001c0001t0003g0239 a0001c0001t0003g0256 a0001c0001t0003g0257 others(2): Show |
5 | NA18957.hp2 NA18971.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-4264A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313514 | |||||||
| chr2:201313576 | G | A | 1 | a0002c0002t0002g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.676-4326C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313576 | |||||||
| chr2:201313642 | A | G | 3 | a0001c0009t0001g0050 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.676-4392T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313642 | |||||||
| chr2:201313674 | C | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-4424G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313674 | |||||||
| chr2:201313684 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.676-4434G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313684 | |||||||
| chr2:201313845 | G | T | 3 | a0002c0002t0004g0210 a0002c0002t0004g0211 a0005c0010t0004g0156 |
3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.676-4595C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313845 | |||||||
| chr2:201313898 | A | G | 6 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(3): Show |
6 | HG00438.hp2 HG02027.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-4648T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313898 | |||||||
| chr2:201313949 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-4699G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313949 | |||||||
| chr2:201313952 | A | G | 70 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(67): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.676-4702T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313952 | |||||||
| chr2:201314035 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-4785G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314035 | |||||||
| chr2:201314287 | T | TA | 77 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(74): Show |
87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.676-5038_676-5037i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314287 | |||||||
| chr2:201314288 | T | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(222): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.676-5038A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314288 | |||||||
| chr2:201314298 | T | A | 16 | a0001c0009t0001g0050 a0002c0003t0005g0214 a0002c0003t0005g0215 others(13): Show |
16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.676-5048A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314298 | |||||||
| chr2:201314375 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0005g0235 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.676-5125T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314375 | |||||||
| chr2:201314420 | T | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(38): Show |
47 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.676-5170A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314420 | |||||||
| chr2:201314461 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.676-5211A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314461 | |||||||
| chr2:201314633 | C | T | 1 | a0002c0002t0002g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.676-5383G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314633 | |||||||
| chr2:201314695 | A | AC | 13 | a0002c0003t0005g0214 a0002c0003t0005g0215 a0002c0003t0005g0219 others(10): Show |
13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-5446_676-5445i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314695 | |||||||
| chr2:201314925 | C | G | 1 | a0001c0001t0003g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676-5675G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314925 | |||||||
| chr2:201315047 | T | G | 3 | a0002c0002t0002g0023 a0002c0002t0002g0170 a0002c0002t0002g0171 |
4 | HG01081.hp2 HG01496.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-5797A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315047 | |||||||
| chr2:201315062 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676-5812T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315062 | |||||||
| chr2:201315254 | A | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.676-6004T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315254 | |||||||
| chr2:201315319 | A | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-6069T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315319 | |||||||
| chr2:201315511 | C | T | 7 | a0002c0002t0002g0160 a0002c0002t0002g0164 a0002c0002t0002g0167 others(4): Show |
7 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-6261G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315511 | |||||||
| chr2:201315522 | T | G | 28 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(25): Show |
29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-6272A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315522 | |||||||
| chr2:201315539 | C | T | 10 | a0002c0003t0005g0219 a0002c0003t0005g0220 a0002c0003t0005g0221 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-6289G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315539 | |||||||
| chr2:201315543 | C | T | 1 | a0002c0002t0002g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676-6293G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315543 | |||||||
| chr2:201315768 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.676-6518A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315768 | |||||||
| chr2:201315994 | C | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.676-6744G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315994 | |||||||
| chr2:201316012 | C | A | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676-6762G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316012 | |||||||
| chr2:201316092 | T | C | 6 | a0001c0001t0003g0010 a0001c0001t0003g0030 a0001c0001t0003g0252 others(3): Show |
9 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-6842A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316092 | |||||||
| chr2:201316117 | A | C | 1 | a0001c0001t0004g0309 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.676-6867T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316117 | |||||||
| chr2:201316435 | C | T | 68 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(65): Show |
77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.676-7185G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316435 | |||||||
| chr2:201316524 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.676-7274G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316524 | |||||||
| chr2:201316561 | A | G | 3 | a0001c0009t0001g0050 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.676-7311T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316561 | |||||||
| chr2:201316580 | C | T | 1 | a0002c0002t0002g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.676-7330G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316580 | |||||||
| chr2:201316637 | G | A | 2 | a0002c0002t0002g0027 a0002c0002t0002g0187 |
3 | HG01358.hp1 HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.676-7387C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316637 | |||||||
| chr2:201316975 | A | C | 3 | a0001c0001t0003g0310 a0001c0001t0011g0313 a0002c0002t0003g0157 |
3 | HG02109.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676-7725T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316975 | |||||||
| chr2:201317030 | G | T | 1 | a0002c0002t0002g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-7780C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317030 | |||||||
| chr2:201317047 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676-7797G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317047 | |||||||
| chr2:201317092 | A | T | 1 | a0001c0001t0003g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.676-7842T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317092 | |||||||
| chr2:201317338 | G | T | 29 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(26): Show |
30 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.676-8088C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317338 | |||||||
| chr2:201317975 | A | G | 1 | a0002c0002t0002g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.676-8725T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317975 | |||||||
| chr2:201318479 | C | T | 2 | a0001c0001t0008g0066 a0001c0001t0008g0067 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.676-9229G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318479 | |||||||
| chr2:201318509 | A | C | 1 | a0002c0003t0005g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.676-9259T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318509 | |||||||
| chr2:201318584 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-9334T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318584 | |||||||
| chr2:201318585 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-9335A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318585 | |||||||
| chr2:201318595 | A | G | 1 | a0001c0001t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.676-9345T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318595 | |||||||
| chr2:201318808 | G | A | 2 | a0001c0001t0003g0266 a0001c0001t0003g0267 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.676-9558C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318808 | |||||||
| chr2:201318931 | G | C | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.676-9681C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318931 | |||||||
| chr2:201318938 | CAG | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.676-9690_676-9689d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318938 | |||||||
| chr2:201319285 | T | G | 2 | a0001c0001t0002g0271 a0002c0002t0002g0165 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.676-10035A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319285 | |||||||
| chr2:201319409 | TA | T | 13 | a0002c0003t0005g0214 a0002c0003t0005g0215 a0002c0003t0005g0219 others(10): Show |
13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-10160delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319409 | |||||||
| chr2:201319442 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(195): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.676-10192G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319442 | |||||||
| chr2:201319492 | A | G | 25 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(22): Show |
26 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-10242T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319492 | |||||||
| chr2:201319608 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.676-10358G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319608 | |||||||
| chr2:201320188 | G | A | 1 | a0001c0001t0003g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.675+10282C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320188 | |||||||
| chr2:201320216 | G | A | 10 | a0002c0003t0005g0219 a0002c0003t0005g0220 a0002c0003t0005g0221 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.675+10254C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320216 | |||||||
| chr2:201320298 | G | A | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.675+10172C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320298 | |||||||
| chr2:201320336 | C | T | 1 | a0001c0001t0004g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.675+10134G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320336 | |||||||
| chr2:201320351 | C | T | 7 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+10119G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320351 | |||||||
| chr2:201320381 | G | A | 1 | a0001c0001t0004g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.675+10089C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320381 | |||||||
| chr2:201320409 | A | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(171): Show |
194 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.675+10061T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320409 | |||||||
| chr2:201320434 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.675+10036G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320434 | |||||||
| chr2:201320439 | C | G | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.675+10031G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320439 | |||||||
| chr2:201320439 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.675+10031G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320439 | |||||||
| chr2:201320566 | T | C | 307 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(304): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.675+9904A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320566 | |||||||
| chr2:201320649 | C | G | 1 | a0001c0001t0006g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.675+9821G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320649 | |||||||
| chr2:201320703 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675+9767G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320703 | |||||||
| chr2:201320709 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.675+9761G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320709 | |||||||
| chr2:201320881 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.675+9589C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320881 | |||||||
| chr2:201321081 | C | T | 3 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0303 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.675+9389G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321081 | |||||||
| chr2:201321105 | A | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+9365T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321105 | |||||||
| chr2:201321238 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.675+9232G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321238 | |||||||
| chr2:201321644 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.675+8826C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321644 | |||||||
| chr2:201321699 | G | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(222): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.675+8771C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321699 | |||||||
| chr2:201321860 | C | T | 1 | a0006c0008t0007g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.675+8610G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321860 | |||||||
| chr2:201322001 | G | C | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+8469C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322001 | |||||||
| chr2:201322039 | C | T | 1 | a0001c0001t0003g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.675+8431G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322039 | |||||||
| chr2:201322042 | G | A | 72 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(69): Show |
81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.675+8428C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322042 | |||||||
| chr2:201322066 | C | T | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+8404G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322066 | |||||||
| chr2:201322072 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.675+8398G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322072 | |||||||
| chr2:201322124 | T | C | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.675+8346A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322124 | |||||||
| chr2:201322262 | T | TA | 3 | a0001c0009t0001g0050 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.675+8207_675+8208i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322262 | |||||||
| chr2:201322263 | C | A | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(241): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.675+8207G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322263 | |||||||
| chr2:201322301 | G | A | 3 | a0002c0002t0004g0210 a0002c0002t0004g0211 a0005c0010t0004g0156 |
3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+8169C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322301 | |||||||
| chr2:201322318 | T | G | 1 | a0002c0002t0002g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.675+8152A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322318 | |||||||
| chr2:201322439 | T | TA | 3 | a0002c0002t0002g0020 a0002c0002t0002g0163 a0002c0002t0002g0213 |
4 | HG00423.hp2 HG02071.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+8030dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322439 | |||||||
| chr2:201322802 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.675+7668C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322802 | |||||||
| chr2:201322900 | A | G | 1 | a0002c0002t0002g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.675+7570T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322900 | |||||||
| chr2:201323055 | A | C | 94 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(91): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+7415T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323055 | |||||||
| chr2:201323135 | A | G | 70 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(67): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.675+7335T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323135 | |||||||
| chr2:201323464 | G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+7006C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323464 | |||||||
| chr2:201323593 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.675+6877G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323593 | |||||||
| chr2:201323784 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0043 others(7): Show |
12 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.675+6678_675+6685d others(10): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(2): Show |
85 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(82): Show |
94 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.675+6677_675+6685d others(11): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0100 others(10): Show |
14 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+6676_675+6685d others(12): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0004g0294 a0001c0001t0007g0070 a0001c0001t0007g0076 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+6675_675+6685d others(13): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(14): Show |
18 | HG02145.hp1 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.675+6674_675+6685d others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0298 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+6673_675+6685d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.675+6671_675+6685d others(17): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0266 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.675+6669_675+6685d others(19): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(11): Show |
7 | a0001c0001t0003g0246 a0001c0001t0003g0267 a0001c0001t0003g0303 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+6668_675+6685d others(20): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(12): Show |
17 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0228 others(14): Show |
19 | HG02717.hp1 HG03239.hp2 HG03490.hp2 others(16): Show |
intron_variant | MODIFIER | c.675+6667_675+6685d others(21): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(13): Show |
21 | a0001c0001t0003g0030 a0001c0001t0003g0230 a0001c0001t0003g0237 others(18): Show |
23 | HG00438.hp2 HG00558.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(14): Show |
21 | a0001c0001t0003g0010 a0001c0001t0003g0031 a0001c0001t0003g0032 others(18): Show |
26 | HG00140.hp2 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(23): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(15): Show |
6 | a0001c0001t0003g0262 a0001c0001t0003g0264 a0001c0001t0003g0265 others(3): Show |
6 | HG02027.hp1 HG03710.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(24): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0011g0313 a0002c0003t0005g0215 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.675+6685_675+6686i others(25): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(18): Show |
2 | a0001c0009t0001g0050 a0002c0003t0005g0227 |
2 | HG01192.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.675+6685_675+6686i others(27): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(21): Show |
1 | a0003c0004t0005g0311 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.675+6685_675+6686i others(30): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | C | CAAAAAAA others(22): Show |
1 | a0003c0004t0005g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.675+6685_675+6686i others(31): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323784 | CA | C | 64 | a0001c0001t0002g0271 a0001c0001t0004g0033 a0001c0001t0008g0066 others(61): Show |
85 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.675+6685delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | |||||||
| chr2:201323804 | G | A | 91 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(88): Show |
101 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.675+6666C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323804 | |||||||
| chr2:201323805 | T | A | 93 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(90): Show |
103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675+6665A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323805 | |||||||
| chr2:201323809 | G | T | 93 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(90): Show |
102 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.675+6661C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323809 | |||||||
| chr2:201323882 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.675+6588G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323882 | |||||||
| chr2:201324016 | G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+6454C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324016 | |||||||
| chr2:201324022 | T | G | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.675+6448A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324022 | |||||||
| chr2:201324037 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+6433G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324037 | |||||||
| chr2:201324046 | T | TAAAAAAG others(164): Show |
1 | a0001c0001t0005g0281 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.675+6423_675+6424i others(173): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324046 | |||||||
| chr2:201324080 | A | G | 70 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(67): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.675+6390T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324080 | |||||||
| chr2:201324119 | T | G | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.675+6351A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324119 | |||||||
| chr2:201324193 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.675+6277G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324193 | |||||||
| chr2:201324206 | C | T | 1 | a0002c0002t0002g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675+6264G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324206 | |||||||
| chr2:201324251 | G | A | 311 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(308): Show |
361 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.675+6219C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324251 | |||||||
| chr2:201324288 | C | A | 1 | a0002c0002t0002g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+6182G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324288 | |||||||
| chr2:201324383 | G | C | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.675+6087C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324383 | |||||||
| chr2:201324546 | T | C | 1 | a0002c0002t0002g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.675+5924A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324546 | |||||||
| chr2:201324593 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.675+5877C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324593 | |||||||
| chr2:201324651 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00323.hp2 HG01243.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.675+5819C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324651 | |||||||
| chr2:201324702 | G | C | 5 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0291 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+5768C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324702 | |||||||
| chr2:201324728 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(100): Show |
114 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.675+5742A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324728 | |||||||
| chr2:201324936 | T | C | 68 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(65): Show |
77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.675+5534A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324936 | |||||||
| chr2:201325001 | G | A | 26 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(23): Show |
27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.675+5469C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325001 | |||||||
| chr2:201325004 | T | C | 26 | a0001c0001t0003g0310 a0001c0001t0006g0014 a0001c0001t0006g0046 others(23): Show |
27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.675+5466A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325004 | |||||||
| chr2:201325098 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+5372G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325098 | |||||||
| chr2:201325141 | A | G | 16 | a0001c0009t0001g0050 a0002c0003t0005g0214 a0002c0003t0005g0215 others(13): Show |
16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.675+5329T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325141 | |||||||
| chr2:201325241 | T | G | 1 | a0001c0001t0012g0314 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.675+5229A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325241 | |||||||
| chr2:201325242 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.675+5228C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325242 | |||||||
| chr2:201325275 | A | C | 94 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(91): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+5195T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325275 | |||||||
| chr2:201325539 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.675+4931C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325539 | |||||||
| chr2:201325731 | ATTCCACC others(5): Show |
A | 1 | a0001c0001t0006g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4727_675+4738d others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325731 | |||||||
| chr2:201325748 | A | C | 1 | a0001c0001t0006g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4722T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325748 | |||||||
| chr2:201325749 | T | A | 1 | a0001c0001t0006g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4721A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325749 | |||||||
| chr2:201325887 | C | T | 18 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(15): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.675+4583G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325887 | |||||||
| chr2:201325945 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.675+4525C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325945 | |||||||
| chr2:201325948 | C | T | 1 | a0001c0001t0005g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+4522G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325948 | |||||||
| chr2:201326227 | TG | T | 18 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(15): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.675+4242delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326227 | |||||||
| chr2:201326526 | C | T | 2 | a0001c0001t0008g0066 a0001c0001t0008g0067 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.675+3944G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326526 | |||||||
| chr2:201326720 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.675+3750G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326720 | |||||||
| chr2:201326913 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0080 others(5): Show |
9 | HG02074.hp1 HG02523.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+3557T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326913 | |||||||
| chr2:201326916 | T | A | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.675+3554A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326916 | |||||||
| chr2:201327046 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+3424G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327046 | |||||||
| chr2:201327067 | T | C | 1 | a0001c0001t0004g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.675+3403A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327067 | |||||||
| chr2:201327123 | T | C | 1 | a0002c0002t0002g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675+3347A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327123 | |||||||
| chr2:201327290 | CA | C | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0145 |
3 | HG02559.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.675+3179delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327290 | |||||||
| chr2:201327351 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.675+3119T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327351 | |||||||
| chr2:201327382 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+3088C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327382 | |||||||
| chr2:201327465 | G | GA | 77 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(74): Show |
87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.675+3004dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327465 | |||||||
| chr2:201327648 | A | G | 17 | a0001c0001t0013g0315 a0001c0009t0001g0050 a0002c0003t0005g0214 others(14): Show |
17 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.675+2822T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327648 | |||||||
| chr2:201327649 | G | GT | 3 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0230 |
3 | NA18950.hp1 NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.675+2820dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327649 | |||||||
| chr2:201327699 | T | G | 94 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(91): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+2771A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327699 | |||||||
| chr2:201327842 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.675+2628T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327842 | |||||||
| chr2:201327920 | GACTAA | G | 3 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0301 |
3 | HG01261.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.675+2545_675+2549d others(7): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327920 | |||||||
| chr2:201327971 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.675+2499G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327971 | |||||||
| chr2:201328012 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.675+2458C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328012 | |||||||
| chr2:201328023 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+2447C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328023 | |||||||
| chr2:201328081 | C | CACTTAAA others(13): Show |
1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.675+2369_675+2388d others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328081 | |||||||
| chr2:201328167 | T | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+2303A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328167 | |||||||
| chr2:201328347 | T | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+2123A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328347 | |||||||
| chr2:201328478 | T | A | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+1992A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328478 | |||||||
| chr2:201328538 | G | A | 1 | a0002c0002t0002g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.675+1932C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328538 | |||||||
| chr2:201328598 | G | A | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0145 |
3 | HG02559.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.675+1872C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328598 | |||||||
| chr2:201328628 | G | A | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.675+1842C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328628 | |||||||
| chr2:201328727 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.675+1743A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328727 | |||||||
| chr2:201328728 | G | A | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.675+1742C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328728 | |||||||
| chr2:201328740 | A | G | 46 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0033 others(43): Show |
54 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.675+1730T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328740 | |||||||
| chr2:201329474 | C | T | 1 | a0002c0002t0002g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.675+996G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329474 | |||||||
| chr2:201329502 | A | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03927.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.675+968T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329502 | |||||||
| chr2:201329529 | C | T | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.675+941G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329529 | |||||||
| chr2:201329736 | T | C | 6 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(3): Show |
6 | HG00438.hp2 HG02027.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+734A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329736 | |||||||
| chr2:201329986 | C | T | 2 | a0002c0002t0002g0176 a0002c0002t0002g0195 |
2 | HG02155.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.675+484G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329986 | |||||||
| chr2:201330047 | G | A | 1 | a0002c0002t0002g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.675+423C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330047 | |||||||
| chr2:201330156 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+314A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330156 | |||||||
| chr2:201330174 | T | C | 1 | a0001c0001t0006g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.675+296A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330174 | |||||||
| chr2:201330209 | T | C | 6 | a0002c0002t0002g0007 a0002c0002t0002g0190 a0002c0002t0002g0197 others(3): Show |
8 | NA18939.hp2 NA18956.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+261A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330209 | |||||||
| chr2:201330213 | A | G | 3 | a0002c0002t0004g0210 a0002c0002t0004g0211 a0005c0010t0004g0156 |
3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+257T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330213 | |||||||
| chr2:201330307 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(119): Show |
133 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.675+163A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330307 | |||||||
| chr2:201330588 | G | A | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-66C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/14 | chr2 | 201330588 | |||||||
| chr2:201330723 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.622+13C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/14 | chr2 | 201330723 | |||||||
| chr2:201330971 | C | CT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG00673.hp2 HG02055.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.525-139dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201330971 | |||||||
| chr2:201331340 | C | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(222): Show |
254 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.525-507G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331340 | |||||||
| chr2:201331561 | G | A | 2 | a0001c0001t0006g0127 a0001c0001t0007g0128 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.525-728C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331561 | |||||||
| chr2:201331567 | C | T | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.525-734G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331567 | |||||||
| chr2:201331672 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.525-839T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331672 | |||||||
| chr2:201331811 | T | C | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525-978A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331811 | |||||||
| chr2:201331829 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.525-996C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331829 | |||||||
| chr2:201331994 | A | G | 66 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(63): Show |
75 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.525-1161T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331994 | |||||||
| chr2:201332166 | G | C | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1333C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332166 | |||||||
| chr2:201332291 | C | T | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-1458G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332291 | |||||||
| chr2:201332726 | C | T | 1 | a0002c0002t0002g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.525-1893G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332726 | |||||||
| chr2:201332826 | CG | C | 3 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0308 |
6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-1994delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332826 | |||||||
| chr2:201332954 | A | T | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2121T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332954 | |||||||
| chr2:201332959 | C | A | 1 | a0002c0002t0002g0023 | 2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.525-2126G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332959 | |||||||
| chr2:201333065 | A | G | 1 | a0001c0001t0004g0005 | 4 | HG02886.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2232T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333065 | |||||||
| chr2:201333225 | G | A | 2 | a0001c0001t0007g0115 a0001c0001t0007g0149 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.525-2392C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333225 | |||||||
| chr2:201333541 | C | T | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2708G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333541 | |||||||
| chr2:201333617 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(187): Show |
211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.525-2784C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333617 | |||||||
| chr2:201333805 | A | T | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-2972T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333805 | |||||||
| chr2:201333866 | C | T | 4 | a0001c0001t0004g0305 a0002c0002t0002g0021 a0002c0002t0002g0024 others(1): Show |
6 | HG01123.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-3033G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333866 | |||||||
| chr2:201333890 | C | A | 2 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
2 | HG01261.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.525-3057G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333890 | |||||||
| chr2:201334040 | C | T | 15 | a0002c0002t0002g0023 a0002c0002t0002g0160 a0002c0002t0002g0164 others(12): Show |
16 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-3207G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334040 | |||||||
| chr2:201334072 | C | G | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-3239G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334072 | |||||||
| chr2:201334114 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.525-3281C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334114 | |||||||
| chr2:201334122 | G | C | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.525-3289C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334122 | |||||||
| chr2:201334185 | G | GT | 311 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(308): Show |
361 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.525-3353_525-3352i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334185 | |||||||
| chr2:201334233 | C | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-3400G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334233 | |||||||
| chr2:201334550 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.525-3717C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334550 | |||||||
| chr2:201334601 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(187): Show |
211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.525-3768A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334601 | |||||||
| chr2:201334732 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(221): Show |
253 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.525-3899T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334732 | |||||||
| chr2:201334782 | TA | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(179): Show |
202 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.525-3950delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334782 | |||||||
| chr2:201334853 | T | C | 1 | a0001c0001t0006g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.525-4020A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334853 | |||||||
| chr2:201334939 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-4106C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334939 | |||||||
| chr2:201334955 | T | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0266 a0001c0001t0003g0267 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.525-4122A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334955 | |||||||
| chr2:201334965 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(182): Show |
205 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.525-4132A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334965 | |||||||
| chr2:201334976 | G | A | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-4143C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334976 | |||||||
| chr2:201335056 | G | A | 1 | a0001c0001t0007g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.525-4223C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335056 | |||||||
| chr2:201335101 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(217): Show |
249 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.525-4268G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335101 | |||||||
| chr2:201335269 | CTA | C | 12 | a0002c0002t0004g0216 a0002c0002t0004g0217 a0002c0003t0005g0219 others(9): Show |
12 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.525-4438_525-4437d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335269 | |||||||
| chr2:201335360 | T | C | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525-4527A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335360 | |||||||
| chr2:201335457 | T | C | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-4624A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335457 | |||||||
| chr2:201335540 | T | C | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.525-4707A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335540 | |||||||
| chr2:201335600 | T | C | 1 | a0001c0001t0008g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.525-4767A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335600 | |||||||
| chr2:201335608 | C | A | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.525-4775G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335608 | |||||||
| chr2:201335608 | C | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(221): Show |
253 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.525-4775G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335608 | |||||||
| chr2:201335699 | T | A | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-4866A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335699 | |||||||
| chr2:201335727 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(256): Show |
289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.525-4894T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335727 | |||||||
| chr2:201335852 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(212): Show |
240 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.525-5019G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335852 | |||||||
| chr2:201335945 | T | A | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-5112A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335945 | |||||||
| chr2:201336007 | G | A | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-5174C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336007 | |||||||
| chr2:201336064 | T | C | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-5231A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336064 | |||||||
| chr2:201336112 | GTGAGCAT others(6): Show |
G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(187): Show |
211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.525-5292_525-5280d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336112 | |||||||
| chr2:201336119 | T | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0286 others(4): Show |
11 | HG01167.hp2 HG01175.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.525-5286A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336119 | |||||||
| chr2:201336180 | C | T | 2 | a0001c0001t0006g0051 a0001c0009t0001g0050 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.525-5347G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336180 | |||||||
| chr2:201336466 | C | T | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-5633G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336466 | |||||||
| chr2:201336622 | C | T | 1 | a0002c0002t0002g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.524+5748G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336622 | |||||||
| chr2:201336729 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.524+5641A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336729 | |||||||
| chr2:201336757 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.524+5613A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336757 | |||||||
| chr2:201336818 | T | C | 1 | a0002c0003t0005g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.524+5552A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336818 | |||||||
| chr2:201337028 | ATTGT | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
210 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.524+5338_524+5341d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337028 | |||||||
| chr2:201337119 | G | A | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+5251C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337119 | |||||||
| chr2:201337356 | G | C | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+5014C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337356 | |||||||
| chr2:201337696 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.524+4674T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337696 | |||||||
| chr2:201337711 | C | T | 8 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(5): Show |
10 | HG00738.hp2 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.524+4659G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337711 | |||||||
| chr2:201337840 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
210 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.524+4530C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337840 | |||||||
| chr2:201337880 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+4490C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337880 | |||||||
| chr2:201337891 | C | T | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+4479G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337891 | |||||||
| chr2:201338068 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
210 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.524+4302T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338068 | |||||||
| chr2:201338340 | C | T | 65 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(62): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+4030G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338340 | |||||||
| chr2:201338341 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.524+4029C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338341 | |||||||
| chr2:201338512 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(217): Show |
249 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.524+3858C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338512 | |||||||
| chr2:201338544 | A | C | 1 | a0002c0002t0002g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.524+3826T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338544 | |||||||
| chr2:201338667 | C | T | 10 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(7): Show |
14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3703G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338667 | |||||||
| chr2:201338864 | G | T | 10 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(7): Show |
14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3506C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338864 | |||||||
| chr2:201339032 | T | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+3338A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339032 | |||||||
| chr2:201339055 | T | TTGTTGGG others(119): Show |
1 | a0001c0001t0006g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.524+3314_524+3315i others(128): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339055 | |||||||
| chr2:201339055 | T | TTGTTGGG others(120): Show |
4 | a0001c0001t0006g0123 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02717.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+3314_524+3315i others(129): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339055 | |||||||
| chr2:201339065 | A | G | 1 | a0001c0001t0007g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.524+3305T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339065 | |||||||
| chr2:201339100 | T | C | 10 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(7): Show |
14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3270A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339100 | |||||||
| chr2:201339378 | C | A | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2992G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339378 | |||||||
| chr2:201339400 | T | C | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+2970A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339400 | |||||||
| chr2:201339473 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.524+2897A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339473 | |||||||
| chr2:201339490 | T | C | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.524+2880A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339490 | |||||||
| chr2:201339692 | T | G | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.524+2678A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339692 | |||||||
| chr2:201339730 | T | C | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+2640A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339730 | |||||||
| chr2:201339794 | C | G | 1 | a0001c0001t0011g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524+2576G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339794 | |||||||
| chr2:201339909 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.524+2461A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339909 | |||||||
| chr2:201340018 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(240): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.524+2352A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340018 | |||||||
| chr2:201340026 | A | G | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.524+2344T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340026 | |||||||
| chr2:201340035 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.524+2335C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340035 | |||||||
| chr2:201340188 | C | T | 1 | a0002c0002t0002g0021 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.524+2182G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340188 | |||||||
| chr2:201340276 | G | T | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2094C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340276 | |||||||
| chr2:201340278 | T | A | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2092A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340278 | |||||||
| chr2:201340287 | T | C | 65 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(62): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+2083A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340287 | |||||||
| chr2:201340399 | A | G | 1 | a0001c0001t0003g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.524+1971T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340399 | |||||||
| chr2:201340474 | C | T | 95 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(92): Show |
112 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.524+1896G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340474 | |||||||
| chr2:201340493 | C | A | 1 | a0001c0001t0007g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.524+1877G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340493 | |||||||
| chr2:201340626 | C | T | 2 | a0001c0001t0007g0069 a0001c0001t0007g0070 |
2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.524+1744G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340626 | |||||||
| chr2:201340717 | G | T | 65 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(62): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+1653C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340717 | |||||||
| chr2:201340797 | C | T | 2 | a0001c0001t0003g0310 a0001c0001t0013g0315 |
2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.524+1573G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340797 | |||||||
| chr2:201341226 | A | G | 3 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0291 |
3 | HG02970.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.524+1144T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341226 | |||||||
| chr2:201341239 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.524+1131A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341239 | |||||||
| chr2:201341392 | C | CAT | 5 | a0002c0002t0002g0164 a0002c0002t0002g0200 a0002c0002t0002g0201 others(2): Show |
5 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+976_524+977dup others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | |||||||
| chr2:201341392 | C | CATAT | 3 | a0002c0002t0002g0020 a0002c0002t0002g0163 a0002c0002t0002g0213 |
4 | HG00423.hp2 HG02071.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+974_524+977dup others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | |||||||
| chr2:201341392 | CAT | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(190): Show |
214 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.524+976_524+977del others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | |||||||
| chr2:201341392 | CATAT | C | 16 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(13): Show |
17 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.524+974_524+977del others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | |||||||
| chr2:201341486 | TAC | T | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+882_524+883del others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341486 | |||||||
| chr2:201341535 | G | GTA | 2 | a0002c0002t0002g0008 a0002c0002t0002g0199 |
4 | HG00544.hp2 HG02040.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+833_524+834dup others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341535 | |||||||
| chr2:201341535 | G | GTATA | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+831_524+834dup others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341535 | |||||||
| chr2:201341597 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(126): Show |
141 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.524+773C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341597 | |||||||
| chr2:201341622 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.524+748T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341622 | |||||||
| chr2:201341849 | T | C | 1 | a0001c0007t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.524+521A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341849 | |||||||
| chr2:201342014 | C | T | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.524+356G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342014 | |||||||
| chr2:201342141 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.524+229A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342141 | |||||||
| chr2:201342212 | T | A | 3 | a0001c0001t0006g0126 a0001c0001t0006g0127 a0001c0001t0007g0128 |
3 | HG02976.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.524+158A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342212 | |||||||
| chr2:201342514 | T | A | 1 | a0001c0001t0004g0301 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.463-83A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342514 | |||||||
| chr2:201342529 | G | A | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.463-98C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342529 | |||||||
| chr2:201342541 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.463-110T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342541 | |||||||
| chr2:201342993 | A | C | 1 | a0001c0001t0003g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.463-562T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342993 | |||||||
| chr2:201343063 | G | A | 1 | a0002c0002t0002g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.463-632C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343063 | |||||||
| chr2:201343270 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(124): Show |
139 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.463-839A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343270 | |||||||
| chr2:201343329 | T | C | 2 | a0001c0001t0004g0306 a0001c0001t0004g0308 |
2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.462+841A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343329 | |||||||
| chr2:201343436 | C | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.462+734G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343436 | |||||||
| chr2:201343515 | T | C | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.462+655A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343515 | |||||||
| chr2:201343672 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.462+498A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343672 | |||||||
| chr2:201343813 | C | T | 1 | a0005c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.462+357G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343813 | |||||||
| chr2:201344087 | G | A | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+83C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201344087 | |||||||
| chr2:201344327 | G | C | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369-64C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201344327 | |||||||
| chr2:201344380 | T | G | 1 | a0001c0001t0004g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.369-117A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201344380 | |||||||
| chr2:201345059 | A | G | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-796T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345059 | |||||||
| chr2:201345254 | C | T | 5 | a0001c0001t0006g0014 a0001c0001t0006g0046 a0001c0001t0006g0047 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-991G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345254 | |||||||
| chr2:201345450 | T | TTG | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0033 others(6): Show |
10 | HG01167.hp2 HG01175.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.368+1090_368+1091d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | T | TTGTG | 3 | a0002c0002t0002g0198 a0002c0002t0002g0199 a0002c0002t0002g0203 |
3 | HG01255.hp2 NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.368+1088_368+1091d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | T | TTGTGTG | 7 | a0001c0001t0001g0132 a0001c0001t0004g0004 a0001c0001t0004g0286 others(4): Show |
10 | HG01515.hp2 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.368+1086_368+1091d others(8): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | TTG | T | 22 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
23 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.368+1090_368+1091d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | TTGTG | T | 5 | a0001c0001t0001g0134 a0001c0001t0002g0271 a0001c0001t0003g0269 others(2): Show |
5 | HG01346.hp2 HG01884.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+1088_368+1091d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | TTGTGTG | T | 76 | a0001c0001t0003g0010 a0001c0001t0003g0028 a0001c0001t0003g0029 others(73): Show |
86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.368+1086_368+1091d others(8): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0003g0310 a0001c0001t0005g0235 a0001c0001t0013g0315 |
3 | HG02083.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.368+1084_368+1091d others(10): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345450 | TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0003g0234 a0003c0004t0005g0311 a0003c0004t0005g0312 |
3 | HG02630.hp1 HG02818.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.368+1082_368+1091d others(12): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | |||||||
| chr2:201345484 | GTA | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0005 a0001c0001t0004g0306 |
6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+1056_368+1057d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345484 | |||||||
| chr2:201345486 | A | G | 3 | a0001c0001t0004g0307 a0001c0001t0004g0308 a0001c0001t0004g0309 |
3 | HG02055.hp1 HG02293.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.368+1056T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345486 | |||||||
| chr2:201345486 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.368+1056T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345486 | |||||||
| chr2:201345663 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.368+879T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345663 | |||||||
| chr2:201345829 | C | T | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.368+713G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345829 | |||||||
| chr2:201345891 | G | A | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.368+651C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345891 | |||||||
| chr2:201345933 | G | A | 1 | a0001c0001t0004g0034 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.368+609C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345933 | |||||||
| chr2:201346184 | A | G | 1 | a0001c0001t0004g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.368+358T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346184 | |||||||
| chr2:201346200 | T | A | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.368+342A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346200 | |||||||
| chr2:201346339 | C | T | 1 | a0001c0001t0005g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.368+203G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346339 | |||||||
| chr2:201346720 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(133): Show |
152 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.235-45G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346720 | |||||||
| chr2:201346735 | ATCT | A | 4 | a0002c0002t0002g0200 a0002c0002t0002g0201 a0002c0002t0002g0202 others(1): Show |
4 | HG01099.hp2 HG01109.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-63_235-61delAG others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346735 | |||||||
| chr2:201346841 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235-166G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346841 | |||||||
| chr2:201346972 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(134): Show |
153 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.235-297C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346972 | |||||||
| chr2:201347152 | CT | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(124): Show |
138 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.235-478delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347152 | |||||||
| chr2:201347377 | C | T | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235-702G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347377 | |||||||
| chr2:201347477 | A | G | 2 | a0002c0002t0005g0158 a0002c0002t0005g0159 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.234+777T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347477 | |||||||
| chr2:201347642 | C | CA | 15 | a0001c0001t0002g0271 a0001c0001t0003g0270 a0002c0002t0004g0216 others(12): Show |
15 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+611dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347642 | |||||||
| chr2:201347642 | C | CAAA | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(126): Show |
142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.234+609_234+611dup others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347642 | |||||||
| chr2:201347651 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(204): Show |
233 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.234+603C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347651 | |||||||
| chr2:201347803 | A | T | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234+451T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347803 | |||||||
| chr2:201347817 | G | A | 1 | a0002c0002t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234+437C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347817 | |||||||
| chr2:201347824 | G | A | 4 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(1): Show |
4 | HG00438.hp2 NA18941.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+430C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347824 | |||||||
| chr2:201347830 | G | A | 1 | a0002c0002t0003g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+424C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347830 | |||||||
| chr2:201347866 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234+388C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347866 | |||||||
| chr2:201348226 | C | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0042 others(2): Show |
6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+28G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201348226 | |||||||
| chr2:201348227 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0042 others(2): Show |
6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+27G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201348227 | |||||||
| chr2:201348338 | C | G | 105 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(102): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.186-36G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348338 | |||||||
| chr2:201348424 | A | AT | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-123dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348424 | |||||||
| chr2:201348437 | T | C | 3 | a0002c0003t0005g0225 a0002c0003t0005g0226 a0002c0003t0005g0227 |
3 | HG01069.hp1 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.186-135A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348437 | |||||||
| chr2:201348635 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.186-333G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348635 | |||||||
| chr2:201348659 | C | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(139): Show |
159 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.186-357G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348659 | |||||||
| chr2:201348745 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.186-443A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348745 | |||||||
| chr2:201348792 | C | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-490G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348792 | |||||||
| chr2:201349112 | T | C | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-810A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349112 | |||||||
| chr2:201349131 | G | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0042 others(2): Show |
6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-829C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349131 | |||||||
| chr2:201349211 | G | A | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-909C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349211 | |||||||
| chr2:201349247 | G | T | 7 | a0001c0001t0003g0028 a0001c0001t0003g0228 a0001c0001t0003g0229 others(4): Show |
8 | HG00621.hp1 NA18950.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-945C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349247 | |||||||
| chr2:201349425 | C | T | 228 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(225): Show |
258 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.186-1123G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349425 | |||||||
| chr2:201349442 | C | T | 1 | a0001c0001t0007g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.186-1140G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349442 | |||||||
| chr2:201349782 | G | A | 13 | a0001c0001t0003g0310 a0001c0001t0004g0004 a0001c0001t0004g0033 others(10): Show |
17 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.185+929C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349782 | |||||||
| chr2:201349945 | C | A | 2 | a0003c0004t0005g0311 a0003c0004t0005g0312 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.185+766G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349945 | |||||||
| chr2:201350123 | C | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 others(5): Show |
8 | HG00558.hp1 HG03927.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+588G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350123 | |||||||
| chr2:201350216 | C | T | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+495G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350216 | |||||||
| chr2:201350321 | G | A | 1 | a0001c0001t0003g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.185+390C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350321 | |||||||
| chr2:201350445 | C | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(154): Show |
175 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.185+266G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350445 | |||||||
| chr2:201350573 | C | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0033 a0001c0001t0004g0284 others(6): Show |
13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+138G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350573 | |||||||
| chr2:201350633 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.185+78C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350633 | |||||||
| chr2:201350686 | C | CAAAACAA others(10): Show |
142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(139): Show |
159 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.185+8_185+24dupTTG others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350686 | |||||||
| chr2:201350844 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0038 |
3 | HG01496.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114-62T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201350844 | |||||||
| chr2:201351096 | T | C | 64 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(61): Show |
73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.113+196A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351096 | |||||||
| chr2:201351116 | G | C | 1 | a0001c0001t0007g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+176C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351116 | |||||||
| chr2:201351117 | C | A | 4 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(1): Show |
4 | HG00438.hp2 NA18941.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+175G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351117 | |||||||
| chr2:201351274 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+18T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351274 | |||||||
| chr2:201351883 | G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-432C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201351883 | |||||||
| chr2:201351938 | G | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(139): Show |
159 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.-47-487C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201351938 | |||||||
| chr2:201352101 | G | A | 4 | a0002c0002t0002g0207 a0002c0002t0002g0208 a0002c0002t0002g0209 others(1): Show |
4 | HG00642.hp2 HG00738.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-650C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352101 | |||||||
| chr2:201352193 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(126): Show |
142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.-47-742C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352193 | |||||||
| chr2:201352242 | G | T | 1 | a0001c0001t0004g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-47-791C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352242 | |||||||
| chr2:201352258 | T | C | 2 | a0002c0002t0004g0210 a0002c0002t0004g0211 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47-807A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352258 | |||||||
| chr2:201352262 | G | C | 65 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(62): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-47-811C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352262 | |||||||
| chr2:201352277 | C | G | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-47-826G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352277 | |||||||
| chr2:201352338 | C | A | 13 | a0001c0001t0003g0310 a0001c0001t0004g0004 a0001c0001t0004g0033 others(10): Show |
17 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-887G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352338 | |||||||
| chr2:201352442 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-991T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352442 | |||||||
| chr2:201352529 | C | T | 1 | a0002c0002t0002g0155 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-47-1078G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352529 | |||||||
| chr2:201352643 | G | C | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-47-1192C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352643 | |||||||
| chr2:201352788 | A | G | 3 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0291 |
3 | HG02970.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-47-1337T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352788 | |||||||
| chr2:201352863 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47-1412C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352863 | |||||||
| chr2:201353063 | C | G | 1 | a0001c0001t0001g0035 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-1612G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353063 | |||||||
| chr2:201353624 | G | A | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2173C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353624 | |||||||
| chr2:201353795 | G | A | 1 | a0001c0001t0003g0032 | 2 | HG00423.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-47-2344C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353795 | |||||||
| chr2:201354248 | G | A | 1 | a0001c0001t0009g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-48+2734C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354248 | |||||||
| chr2:201354301 | G | C | 1 | a0001c0001t0004g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-48+2681C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354301 | |||||||
| chr2:201354316 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(140): Show |
160 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-48+2666T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354316 | |||||||
| chr2:201354415 | A | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48+2567T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354415 | |||||||
| chr2:201354596 | G | A | 64 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(61): Show |
73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+2386C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354596 | |||||||
| chr2:201354604 | C | A | 1 | a0001c0001t0007g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-48+2378G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354604 | |||||||
| chr2:201354897 | G | A | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48+2085C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354897 | |||||||
| chr2:201354929 | T | C | 6 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(3): Show |
9 | HG02055.hp1 HG02293.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+2053A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354929 | |||||||
| chr2:201355055 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-48+1927G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355055 | |||||||
| chr2:201355072 | G | A | 64 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(61): Show |
73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+1910C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355072 | |||||||
| chr2:201355317 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-48+1665G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355317 | |||||||
| chr2:201355358 | G | T | 56 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(53): Show |
63 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-48+1624C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355358 | |||||||
| chr2:201355737 | G | C | 15 | a0001c0001t0004g0034 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48+1245C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355737 | |||||||
| chr2:201355895 | C | T | 65 | a0001c0001t0002g0271 a0001c0001t0003g0010 a0001c0001t0003g0028 others(62): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-48+1087G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355895 | |||||||
| chr2:201355900 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(226): Show |
259 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.-48+1082A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355900 | |||||||
| chr2:201356042 | G | C | 6 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(3): Show |
9 | HG02055.hp1 HG02293.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+940C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356042 | |||||||
| chr2:201356082 | G | A | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+900C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356082 | |||||||
| chr2:201356120 | G | A | 1 | a0004c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-48+862C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356120 | |||||||
| chr2:201356252 | C | T | 1 | a0001c0001t0003g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-48+730G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356252 | |||||||
| chr2:201356264 | G | A | 1 | a0001c0001t0004g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+718C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356264 | |||||||
| chr2:201356321 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-48+661A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356321 | |||||||
| chr2:201356515 | GCTT | G | 14 | a0002c0002t0004g0216 a0002c0002t0004g0217 a0002c0003t0005g0214 others(11): Show |
14 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48+464_-48+466del others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356515 | |||||||
| chr2:201356583 | T | C | 5 | a0001c0001t0004g0005 a0001c0001t0004g0306 a0001c0001t0004g0307 others(2): Show |
8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+399A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356583 | |||||||
| chr2:201356645 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+337A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356645 | |||||||
| chr2:201356656 | G | A | 4 | a0001c0001t0003g0310 a0001c0001t0013g0315 a0003c0004t0005g0311 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+326C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356656 | |||||||
| chr2:201356718 | T | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(225): Show |
258 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.-48+264A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356718 | |||||||
| chr2:201356812 | AT | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(126): Show |
142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.-48+169delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356812 |