Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23360 |
| ensemblid | ENSG00000109920.13 |
| hgncid | 19752 |
| symbol | FNBP4 |
| name | formin binding protein 4 |
| refseq_nuc | NM_015308.5 |
| refseq_prot | NP_056123.2 |
| ensembl_nuc | ENST00000263773.10 |
| ensembl_prot | ENSP00000263773.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47716494 |
| end | 47767341 |
| strand | - |
| ver | v1.2 |
| region | chr11:47716494-47767341 |
| region5000 | chr11:47711494-47772341 |
| regionname0 | FNBP4_chr11_47716494_47767341 |
| regionname5000 | FNBP4_chr11_47711494_47772341 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1017 | 233 | 73 | 36 | 94 | 6 | 22 | 81 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0002 | 0/0 | 1015 | 101 | 8 | 28 | 36 | 8 | 21 | 25 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1010): Show |
chr11 | 47711494 | 47772341 |
| a0003 | 0/0 | 1015 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1010): Show |
chr11 | 47711494 | 47772341 |
| a0004 | 0/0 | 1017 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0005 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0006 | 0/0 | 1015 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1010): Show |
chr11 | 47711494 | 47772341 |
| a0007 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0008 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0009 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| a0010 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | MGKKS others(1012): Show |
chr11 | 47711494 | 47772341 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3051 | 219 | 69 | 34 | 87 | 6 | 21 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0005 | 0/0 | 3051 | 7 | 0 | 0 | 6 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0007 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0010 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0011 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0013 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0001c0015 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0002 | 0/0 | 3045 | 82 | 8 | 19 | 33 | 4 | 18 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0003 | 0/0 | 3045 | 12 | 0 | 8 | 0 | 2 | 2 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0006 | 0/0 | 3045 | 3 | 0 | 1 | 2 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0009 | 0/0 | 3045 | 2 | 0 | 0 | 0 | 2 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0020 | 0/0 | 3045 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0002c0021 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0003c0004 | 0/0 | 3045 | 8 | 0 | 0 | 8 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0004c0008 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0005c0014 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0006c0019 | 0/0 | 3045 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3040): Show |
chr11 | 47711494 | 47772341 | ||
| a0007c0018 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0008c0012 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0009c0017 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 | ||
| a0010c0016 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | ATGGG others(3046): Show |
chr11 | 47711494 | 47772341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4035 | 219 | 69 | 34 | 87 | 6 | 21 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0005t0001 | 0/0 | 4035 | 7 | 0 | 0 | 6 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0007t0001 | 0/0 | 4035 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0010t0001 | 0/0 | 4035 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0011t0001 | 0/0 | 4035 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0013t0001 | 0/0 | 4035 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0001c0015t0001 | 0/0 | 4035 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0002c0002t0001 | 0/0 | 4029 | 81 | 8 | 18 | 33 | 4 | 18 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0002t0002 | 0/0 | 4029 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0003t0001 | 0/0 | 4029 | 12 | 0 | 8 | 0 | 2 | 2 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0006t0001 | 0/0 | 4029 | 3 | 0 | 1 | 2 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0009t0001 | 0/0 | 4029 | 2 | 0 | 0 | 0 | 2 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0020t0001 | 0/0 | 4029 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0002c0021t0001 | 0/0 | 4029 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0003c0004t0001 | 0/0 | 4029 | 8 | 0 | 0 | 8 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0004c0008t0001 | 0/0 | 4035 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0005c0014t0001 | 0/0 | 4035 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0006c0019t0001 | 0/0 | 4029 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4024): Show |
chr11 | 47711494 | 47772341 |
| a0007c0018t0001 | 0/0 | 4035 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0008c0012t0001 | 0/0 | 4035 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0009c0017t0001 | 0/0 | 4035 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| a0010c0016t0001 | 0/0 | 4035 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | AGTGC others(4030): Show |
chr11 | 47711494 | 47772341 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0007t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0007t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0010t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0010t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0011t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0013t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0001c0015t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0006t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0009t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0020t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0002c0021t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0003c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0004c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0004c0008t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0005c0014t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0006c0019t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0007c0018t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0008c0012t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0009c0017t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| a0010c0016t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0323 | EUR | GBR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0316 | EUR | GBR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00280 | hp2 | a0002 | c0009 | t0001 | g0255 | EUR | FIN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0249 | EUR | FIN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00544 | hp1 | a0002 | c0006 | t0001 | g0315 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0318 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0241 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0259 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0243 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0246 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0263 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0253 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0329 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0321 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0328 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01496 | hp1 | a0001 | c0013 | t0001 | g0139 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0258 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01517 | hp1 | a0002 | c0009 | t0001 | g0242 | EUR | IBS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0288 | EUR | IBS | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01978 | hp2 | a0002 | c0006 | t0001 | g0289 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0260 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02083 | hp2 | a0003 | c0004 | t0001 | g0339 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | CDX | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02258 | hp1 | a0001 | c0010 | t0001 | g0346 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02280 | hp1 | a0005 | c0014 | t0001 | g0195 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02293 | hp1 | a0001 | c0015 | t0001 | g0125 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0265 | AMR | PEL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0239 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0322 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02683 | hp2 | a0006 | c0019 | t0001 | g0319 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02896 | hp1 | a0004 | c0008 | t0001 | g0035 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0004 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02897 | hp1 | a0001 | c0007 | t0001 | g0005 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02970 | hp2 | a0001 | c0010 | t0001 | g0345 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0277 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03098 | hp1 | a0004 | c0008 | t0001 | g0034 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03654 | hp2 | a0002 | c0020 | t0001 | g0262 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0257 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0296 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0278 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0227 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0269 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | BEB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18747 | hp2 | a0007 | c0018 | t0001 | g0182 | EAS | CHB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18940 | hp2 | a0003 | c0004 | t0001 | g0341 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18942 | hp1 | a0003 | c0004 | t0001 | g0342 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0343 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18949 | hp1 | a0002 | c0021 | t0001 | g0293 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18952 | hp2 | a0001 | c0005 | t0001 | g0229 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18981 | hp1 | a0003 | c0004 | t0001 | g0344 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18983 | hp1 | a0001 | c0005 | t0001 | g0098 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18991 | hp2 | a0008 | c0012 | t0001 | g0197 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18993 | hp1 | a0003 | c0004 | t0001 | g0337 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18999 | hp2 | a0001 | c0005 | t0001 | g0099 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19002 | hp1 | a0009 | c0017 | t0001 | g0128 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19006 | hp2 | a0001 | c0011 | t0001 | g0224 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0340 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19063 | hp1 | a0001 | c0005 | t0001 | g0228 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19078 | hp2 | a0010 | c0016 | t0001 | g0095 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19080 | hp1 | a0001 | c0005 | t0001 | g0230 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19080 | hp2 | a0001 | c0005 | t0001 | g0170 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0338 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | ASW | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ASW | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0256 | EUR | TSI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0297 | EUR | TSI | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | GIH | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0317 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | CLM | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA18955 | hp2 | a0002 | c0006 | t0001 | g0294 | EAS | JPT | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0129 | REF | REF | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | FNBP4_chr11_47711494_47772341 | FNBP4 | chr11 | 47711494 | 47772341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47723083 | C | T | 1 | a0008 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2698G>A | p.Ala900Thr | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/17 | 2751/4035 | 2698/3054 | 900/1017 | chr11 | 47723083 | |||
| chr11:47724037 | T | C | 1 | a0002 | 12 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(9): Show |
missense_variant | MODERATE | c.2455A>G | p.Ile819Val | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/17 | 2508/4035 | 2455/3054 | 819/1017 | chr11 | 47724037 | |||
| chr11:47724112 | T | C | 1 | a0004 | 2 | HG02896.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.2380A>G | p.Thr794Ala | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/17 | 2433/4035 | 2380/3054 | 794/1017 | chr11 | 47724112 | |||
| chr11:47724472 | C | A | 1 | a0005 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2315G>T | p.Ser772Ile | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 13/17 | 2368/4035 | 2315/3054 | 772/1017 | chr11 | 47724472 | |||
| chr11:47746110 | C | G | 1 | a0006 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.1191G>C | p.Glu397Asp | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/17 | 1244/4035 | 1191/3054 | 397/1017 | chr11 | 47746110 | |||
| chr11:47746156 | G | A | 1 | a0006 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.1145C>T | p.Pro382Leu | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/17 | 1198/4035 | 1145/3054 | 382/1017 | chr11 | 47746156 | |||
| chr11:47750993 | T | C | 1 | a0002 | 3 | HG00544.hp1 HG01978.hp2 NA18955.hp2 |
missense_variant | MODERATE | c.829A>G | p.Ile277Val | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/17 | 882/4035 | 829/3054 | 277/1017 | chr11 | 47750993 | |||
| chr11:47751159 | G | C | 1 | a0002 | 2 | HG00280.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.769C>G | p.Gln257Glu | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 5/17 | 822/4035 | 769/3054 | 257/1017 | chr11 | 47751159 | |||
| chr11:47753027 | G | A | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.526C>T | p.Pro176Ser | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/17 | 579/4035 | 526/3054 | 176/1017 | chr11 | 47753027 | |||
| chr11:47765314 | G | T | 1 | a0009 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.269C>A | p.Pro90Gln | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/17 | 322/4035 | 269/3054 | 90/1017 | chr11 | 47765314 | |||
| chr11:47765317 | G | A | 1 | a0009 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.266C>T | p.Pro89Leu | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/17 | 319/4035 | 266/3054 | 89/1017 | chr11 | 47765317 | |||
| chr11:47765350 | G | A | 2 | a0002 a0007 |
2 | NA18747.hp2 NA18949.hp1 |
missense_variant | MODERATE | c.233C>T | p.Ala78Val | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/17 | 286/4035 | 233/3054 | 78/1017 | chr11 | 47765350 | |||
| chr11:47767111 | CGGTGGT | C | 3 | a0002 a0003 a0006 |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
conservative_inframe_deletion | MODERATE | c.172_177delACCACC | p.Thr58_Thr59del | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/17 | 230/4035 | 172/3054 | 58/1017 | chr11 | 47767111 | |||
| chr11:47767143 | G | C | 1 | a0003 | 8 | HG02083.hp2 NA18940.hp2 NA18942.hp1 others(5): Show |
missense_variant | MODERATE | c.146C>G | p.Pro49Arg | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/17 | 199/4035 | 146/3054 | 49/1017 | chr11 | 47767143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47720081 | C | T | 1 | a0001c0013 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.2811G>A | p.Lys937Lys | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/17 | 2864/4035 | 2811/3054 | 937/1017 | chr11 | 47720081 | |||
| chr11:47723057 | T | A | 1 | a0001c0005 | 7 | HG03942.hp2 NA18952.hp2 NA18983.hp1 others(4): Show |
synonymous_variant | LOW | c.2724A>T | p.Pro908Pro | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/17 | 2777/4035 | 2724/3054 | 908/1017 | chr11 | 47723057 | |||
| chr11:47746221 | T | C | 2 | a0001c0015 a0002c0020 |
2 | HG02293.hp1 HG03654.hp2 |
synonymous_variant | LOW | c.1080A>G | p.Thr360Thr | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/17 | 1133/4035 | 1080/3054 | 360/1017 | chr11 | 47746221 | |||
| chr11:47765316 | A | G | 1 | a0009c0017 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.267T>C | p.Pro89Pro | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/17 | 320/4035 | 267/3054 | 89/1017 | chr11 | 47765316 | |||
| chr11:47765349 | C | G | 1 | a0001c0011 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.234G>C | p.Ala78Ala | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/17 | 287/4035 | 234/3054 | 78/1017 | chr11 | 47765349 | |||
| chr11:47767112 | G | A | 1 | a0001c0001 | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
synonymous_variant | LOW | c.177C>T | p.Thr59Thr | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/17 | 230/4035 | 177/3054 | 59/1017 | chr11 | 47767112 | |||
| chr11:47767211 | C | A | 1 | a0001c0010 | 2 | HG02258.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.78G>T | p.Thr26Thr | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/17 | 131/4035 | 78/3054 | 26/1017 | chr11 | 47767211 | |||
| chr11:47767256 | A | G | 1 | a0001c0007 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.33T>C | p.Arg11Arg | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/17 | 86/4035 | 33/3054 | 11/1017 | chr11 | 47767256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47716982 | G | A | 1 | a0002c0002t0002 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 17/17 | 440 | chr11 | 47716982 | ||||||
| chr11:47717007 | G | A | 1 | a0002c0002t0002 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 17/17 | 415 | chr11 | 47717007 | ||||||
| chr11:47717024 | T | A | 1 | a0002c0002t0002 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 17/17 | 398 | chr11 | 47717024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47717563 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2964-51C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717563 | |||||||
| chr11:47717621 | CTA | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2964-111_2964-110d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717621 | |||||||
| chr11:47717667 | TCTTCATC others(27): Show |
T | 1 | a0002c0002t0001g0313 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2964-189_2964-156d others(36): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717667 | |||||||
| chr11:47717763 | A | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | NA18747.hp1 NA18943.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.2964-251T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717763 | |||||||
| chr11:47717771 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2964-259C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717771 | |||||||
| chr11:47717933 | TA | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0047 others(61): Show |
66 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2964-422delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717933 | |||||||
| chr11:47717934 | A | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0029 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2964-422T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47717934 | |||||||
| chr11:47718041 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0065 others(9): Show |
12 | HG02523.hp2 NA18982.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.2964-529G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718041 | |||||||
| chr11:47718045 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2964-533C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718045 | |||||||
| chr11:47718050 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2964-538G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718050 | |||||||
| chr11:47718214 | G | GT | 14 | a0001c0001t0001g0091 a0002c0003t0001g0239 a0002c0003t0001g0241 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2964-703dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718214 | |||||||
| chr11:47718326 | G | T | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2964-814C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718326 | |||||||
| chr11:47718508 | G | A | 6 | a0001c0005t0001g0098 a0001c0005t0001g0099 a0001c0005t0001g0227 others(3): Show |
6 | HG03942.hp2 NA18952.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2964-996C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718508 | |||||||
| chr11:47718550 | A | T | 1 | a0002c0002t0001g0313 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2964-1038T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718550 | |||||||
| chr11:47718794 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2963+1135C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718794 | |||||||
| chr11:47718905 | G | GT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
144 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.2963+1023dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718905 | |||||||
| chr11:47718905 | G | GTT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0150 a0001c0001t0001g0155 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2963+1022_2963+102 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718905 | |||||||
| chr11:47718999 | G | A | 16 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0082 others(13): Show |
16 | HG00673.hp2 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2963+930C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47718999 | |||||||
| chr11:47719073 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2963+856T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719073 | |||||||
| chr11:47719110 | G | A | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2963+819C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719110 | |||||||
| chr11:47719128 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2963+801A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719128 | |||||||
| chr11:47719135 | G | A | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2963+794C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719135 | |||||||
| chr11:47719151 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2963+778C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719151 | |||||||
| chr11:47719179 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2963+750A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719179 | |||||||
| chr11:47719568 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2963+361T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719568 | |||||||
| chr11:47719568 | ATGTGTGT others(11): Show |
A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01069.hp2 HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2963+343_2963+360d others(20): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719568 | |||||||
| chr11:47719576 | A | ATG | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(13): Show |
16 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2963+351_2963+352d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | A | ATGTG | 19 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0025 others(16): Show |
19 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2963+349_2963+352d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0009 a0004c0008t0001g0034 a0004c0008t0001g0035 |
3 | HG02896.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2963+343_2963+352d others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2963+339_2963+352d others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2963+353T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATG | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2963+351_2963+352d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTG | A | 47 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0051 others(44): Show |
47 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2963+349_2963+352d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTG | A | 12 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0080 others(9): Show |
12 | HG01109.hp2 HG01169.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.2963+347_2963+352d others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTGT others(1): Show |
A | 75 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2963+345_2963+352d others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTGT others(3): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | NA18945.hp1 NA18949.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.2963+343_2963+352d others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTGT others(5): Show |
A | 2 | a0002c0002t0001g0244 a0002c0002t0001g0245 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2963+341_2963+352d others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTGT others(7): Show |
A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.2963+339_2963+352d others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719576 | ATGTGTGT others(9): Show |
A | 3 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 |
3 | HG01175.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2963+337_2963+352d others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719576 | |||||||
| chr11:47719651 | G | A | 17 | a0002c0002t0001g0307 a0002c0002t0001g0308 a0002c0002t0001g0309 others(14): Show |
17 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.2963+278C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719651 | |||||||
| chr11:47719714 | T | C | 30 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2963+215A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719714 | |||||||
| chr11:47719831 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0106 |
2 | HG00140.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.2963+98T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719831 | |||||||
| chr11:47719832 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0025 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2963+97A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 16/16 | chr11 | 47719832 | |||||||
| chr11:47720151 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2806-65T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720151 | |||||||
| chr11:47720192 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2806-106G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720192 | |||||||
| chr11:47720307 | G | A | 1 | a0002c0002t0001g0322 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2806-221C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720307 | |||||||
| chr11:47720324 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2806-238A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720324 | |||||||
| chr11:47720427 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2806-341T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720427 | |||||||
| chr11:47720569 | A | AAAAT | 37 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0103 others(34): Show |
37 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.2806-487_2806-484d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720569 | |||||||
| chr11:47720569 | AAAAT | A | 80 | a0002c0002t0001g0235 a0002c0002t0001g0266 a0002c0002t0001g0267 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2806-487_2806-484d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720569 | |||||||
| chr11:47720573 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0213 |
2 | HG02273.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2806-487A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720573 | |||||||
| chr11:47720577 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2806-491A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720577 | |||||||
| chr11:47720603 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0217 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2806-517G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720603 | |||||||
| chr11:47720688 | T | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2806-602A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720688 | |||||||
| chr11:47720722 | C | T | 1 | a0002c0002t0001g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2806-636G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720722 | |||||||
| chr11:47720766 | T | TA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0052 others(26): Show |
30 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2806-681dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720766 | |||||||
| chr11:47720766 | TA | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0070 others(7): Show |
10 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2806-681delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720766 | |||||||
| chr11:47720793 | T | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2806-707A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720793 | |||||||
| chr11:47720839 | C | G | 1 | a0002c0002t0001g0313 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2806-753G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720839 | |||||||
| chr11:47720848 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2806-762G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720848 | |||||||
| chr11:47720983 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0188 a0001c0001t0001g0193 |
3 | HG01261.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2806-897G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47720983 | |||||||
| chr11:47721087 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2806-1001G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721087 | |||||||
| chr11:47721093 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2806-1007C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721093 | |||||||
| chr11:47721167 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2806-1081T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721167 | |||||||
| chr11:47721290 | A | G | 1 | a0002c0002t0002g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2806-1204T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721290 | |||||||
| chr11:47721701 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2805+1275T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721701 | |||||||
| chr11:47721914 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2805+1062A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721914 | |||||||
| chr11:47721915 | T | TA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0043 others(86): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2805+1060dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47721915 | |||||||
| chr11:47722007 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2805+959_2805+968d others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(6): Show |
C | 2 | a0002c0002t0001g0270 a0002c0002t0001g0313 |
2 | NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2805+956_2805+968d others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2805+955_2805+968d others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(8): Show |
C | 4 | a0002c0002t0001g0247 a0002c0002t0001g0291 a0002c0002t0001g0292 others(1): Show |
4 | HG00673.hp1 HG03139.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2805+954_2805+968d others(17): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(9): Show |
C | 34 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0044 others(31): Show |
34 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.2805+953_2805+968d others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(10): Show |
C | 67 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0042 others(64): Show |
67 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2805+952_2805+968d others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(11): Show |
C | 83 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0033 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.2805+951_2805+968d others(20): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0085 a0005c0014t0001g0195 |
3 | HG02280.hp1 HG03486.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2805+950_2805+968d others(21): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(13): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(6): Show |
9 | HG02293.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2805+949_2805+968d others(22): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(14): Show |
C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2805+948_2805+968d others(23): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(15): Show |
C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0063 others(6): Show |
9 | HG02148.hp2 HG02559.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2805+947_2805+968d others(24): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(16): Show |
C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0047 others(25): Show |
30 | HG00544.hp2 HG00597.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2805+946_2805+968d others(25): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(17): Show |
C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(69): Show |
73 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.2805+945_2805+968d others(26): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2805+943_2805+968d others(28): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722007 | CAAAAAAA others(21): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2805+941_2805+968d others(30): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722007 | |||||||
| chr11:47722034 | AAAAAAAA others(13): Show |
A | 1 | a0001c0010t0001g0345 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2805+922_2805+941d others(22): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722034 | |||||||
| chr11:47722035 | AAAAAAAA others(12): Show |
A | 1 | a0001c0010t0001g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2805+922_2805+940d others(21): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722035 | |||||||
| chr11:47722053 | A | G | 85 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2805+923T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722053 | |||||||
| chr11:47722055 | G | A | 85 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2805+921C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722055 | |||||||
| chr11:47722056 | A | G | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2805+920T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722056 | |||||||
| chr11:47722114 | G | A | 1 | a0002c0002t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2805+862C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722114 | |||||||
| chr11:47722132 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2805+844G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722132 | |||||||
| chr11:47722144 | G | GT | 9 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0056 others(6): Show |
9 | HG02056.hp1 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2805+831dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722144 | |||||||
| chr11:47722144 | G | GTT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2805+830_2805+831d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722144 | |||||||
| chr11:47722144 | GT | G | 82 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2805+831delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722144 | |||||||
| chr11:47722253 | CT | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(335): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2805+722delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722253 | |||||||
| chr11:47722349 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2805+627T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722349 | |||||||
| chr11:47722553 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2805+423T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722553 | |||||||
| chr11:47722585 | T | C | 4 | a0002c0002t0001g0267 a0002c0002t0001g0268 a0002c0002t0001g0277 others(1): Show |
4 | HG01071.hp1 HG03017.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2805+391A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722585 | |||||||
| chr11:47722815 | T | C | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0264 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2805+161A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722815 | |||||||
| chr11:47722842 | C | A | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2805+134G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722842 | |||||||
| chr11:47722877 | C | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.2805+99G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 15/16 | chr11 | 47722877 | |||||||
| chr11:47723628 | G | T | 1 | a0002c0002t0001g0311 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2465-312C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723628 | |||||||
| chr11:47723651 | A | G | 1 | a0002c0002t0001g0316 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2465-335T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723651 | |||||||
| chr11:47723727 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2464+301C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723727 | |||||||
| chr11:47723771 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2464+257G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723771 | |||||||
| chr11:47723806 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0166 others(5): Show |
9 | HG01261.hp2 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2464+222C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723806 | |||||||
| chr11:47723822 | C | T | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2464+206G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47723822 | |||||||
| chr11:47724017 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0220 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2464+11A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 14/16 | chr11 | 47724017 | |||||||
| chr11:47724301 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2320-129G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 13/16 | chr11 | 47724301 | |||||||
| chr11:47724376 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2319+92G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 13/16 | chr11 | 47724376 | |||||||
| chr11:47725062 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2009-284G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47725062 | |||||||
| chr11:47725410 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0052 others(14): Show |
18 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2009-632T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47725410 | |||||||
| chr11:47725513 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02809.hp2 HG02897.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009-735G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47725513 | |||||||
| chr11:47726199 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0204 |
2 | NA18941.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.2009-1421C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726199 | |||||||
| chr11:47726257 | T | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2009-1479A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726257 | |||||||
| chr11:47726407 | A | AT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2009-1630dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726407 | |||||||
| chr11:47726407 | A | ATT | 8 | a0001c0001t0001g0043 a0001c0001t0001g0078 a0001c0001t0001g0101 others(5): Show |
8 | HG01884.hp1 HG01943.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-1631_2009-163 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726407 | |||||||
| chr11:47726407 | AT | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009-1630delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726407 | |||||||
| chr11:47726407 | ATTTTTT | A | 107 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2009-1635_2009-163 others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726407 | |||||||
| chr11:47726466 | C | T | 1 | a0002c0002t0001g0277 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2009-1688G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726466 | |||||||
| chr11:47726467 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009-1689C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726467 | |||||||
| chr11:47726470 | T | C | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2009-1692A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726470 | |||||||
| chr11:47726543 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2009-1765A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726543 | |||||||
| chr11:47726720 | A | G | 1 | a0002c0002t0001g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2009-1942T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726720 | |||||||
| chr11:47726783 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2009-2005G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726783 | |||||||
| chr11:47726801 | T | C | 30 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2009-2023A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726801 | |||||||
| chr11:47726957 | T | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.2009-2179A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47726957 | |||||||
| chr11:47727244 | T | G | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2009-2466A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47727244 | |||||||
| chr11:47727251 | C | CT | 10 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0076 others(7): Show |
10 | HG02056.hp1 HG02523.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009-2474dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47727251 | |||||||
| chr11:47727251 | C | CTT | 104 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2009-2475_2009-247 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47727251 | |||||||
| chr11:47727272 | C | T | 24 | a0002c0002t0001g0237 a0002c0002t0001g0244 a0002c0002t0001g0245 others(21): Show |
24 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.2009-2494G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47727272 | |||||||
| chr11:47727417 | T | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2009-2639A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47727417 | |||||||
| chr11:47728028 | G | A | 3 | a0002c0006t0001g0289 a0002c0006t0001g0294 a0002c0006t0001g0315 |
3 | HG00544.hp1 HG01978.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.2009-3250C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728028 | |||||||
| chr11:47728192 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2008+3182G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728192 | |||||||
| chr11:47728352 | C | T | 12 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0210 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2008+3022G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728352 | |||||||
| chr11:47728403 | C | A | 1 | a0002c0021t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2008+2971G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728403 | |||||||
| chr11:47728406 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2008+2968G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728406 | |||||||
| chr11:47728408 | C | T | 83 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.2008+2966G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728408 | |||||||
| chr11:47728578 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0104 |
2 | NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2008+2796G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728578 | |||||||
| chr11:47728671 | G | A | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2008+2703C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728671 | |||||||
| chr11:47728848 | C | CT | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2008+2525dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728848 | |||||||
| chr11:47728848 | C | CTT | 28 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0039 others(25): Show |
28 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.2008+2524_2008+252 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728848 | |||||||
| chr11:47728848 | C | CTTT | 6 | a0001c0001t0001g0025 a0002c0002t0001g0237 a0002c0003t0001g0241 others(3): Show |
6 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2008+2523_2008+252 others(7): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47728848 | |||||||
| chr11:47729060 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2008+2314G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47729060 | |||||||
| chr11:47729109 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(9): Show |
12 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2008+2265G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47729109 | |||||||
| chr11:47729314 | C | T | 1 | a0002c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2008+2060G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47729314 | |||||||
| chr11:47729841 | T | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.2008+1533A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47729841 | |||||||
| chr11:47729985 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2008+1389G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47729985 | |||||||
| chr11:47730407 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2008+967C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47730407 | |||||||
| chr11:47730572 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2008+802G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47730572 | |||||||
| chr11:47730865 | T | C | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2008+509A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47730865 | |||||||
| chr11:47731193 | A | G | 1 | a0003c0004t0001g0342 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2008+181T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47731193 | |||||||
| chr11:47731223 | A | G | 83 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.2008+151T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47731223 | |||||||
| chr11:47731304 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2008+70A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 12/16 | chr11 | 47731304 | |||||||
| chr11:47731802 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1821-241A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 11/16 | chr11 | 47731802 | |||||||
| chr11:47731818 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1821-257G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 11/16 | chr11 | 47731818 | |||||||
| chr11:47732792 | G | C | 1 | a0002c0020t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1687-122C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47732792 | |||||||
| chr11:47732806 | C | A | 1 | a0002c0002t0001g0270 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1687-136G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47732806 | |||||||
| chr11:47732855 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1687-185G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47732855 | |||||||
| chr11:47732888 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1687-218G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47732888 | |||||||
| chr11:47733097 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1687-427C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733097 | |||||||
| chr11:47733331 | T | C | 1 | a0001c0015t0001g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1687-661A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733331 | |||||||
| chr11:47733377 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(332): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1686+648A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733377 | |||||||
| chr11:47733413 | G | A | 3 | a0001c0001t0001g0087 a0002c0002t0001g0334 a0002c0002t0001g0335 |
3 | NA18956.hp1 NA18956.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1686+612C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733413 | |||||||
| chr11:47733496 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02809.hp2 HG02897.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1686+529G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733496 | |||||||
| chr11:47733585 | C | T | 1 | a0002c0003t0001g0257 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1686+440G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733585 | |||||||
| chr11:47733733 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1686+292A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733733 | |||||||
| chr11:47733747 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1686+278A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733747 | |||||||
| chr11:47733964 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1686+61T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47733964 | |||||||
| chr11:47734000 | C | CA | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1686+24dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47734000 | |||||||
| chr11:47734000 | C | CAA | 10 | a0001c0001t0001g0044 a0001c0001t0001g0089 a0001c0001t0001g0091 others(7): Show |
10 | HG00642.hp1 HG01358.hp1 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.1686+23_1686+24dup others(2): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 10/16 | chr11 | 47734000 | |||||||
| chr11:47734469 | A | C | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1582-340T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734469 | |||||||
| chr11:47734561 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1582-432T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734561 | |||||||
| chr11:47734769 | T | TA | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1582-641dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734769 | |||||||
| chr11:47734810 | T | C | 1 | a0002c0003t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1582-681A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734810 | |||||||
| chr11:47734852 | A | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0217 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1582-723T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734852 | |||||||
| chr11:47734865 | C | T | 1 | a0002c0002t0001g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1582-736G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734865 | |||||||
| chr11:47734923 | A | C | 85 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1582-794T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734923 | |||||||
| chr11:47734986 | C | A | 1 | a0002c0002t0001g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1582-857G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734986 | |||||||
| chr11:47734988 | C | CA | 77 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(74): Show |
77 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1582-860_1582-859i others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734988 | |||||||
| chr11:47734989 | C | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1582-860G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734989 | |||||||
| chr11:47734989 | C | CA | 44 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(41): Show |
44 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1582-861dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47734989 | |||||||
| chr11:47735013 | C | T | 3 | a0002c0002t0001g0334 a0002c0002t0001g0335 a0002c0002t0001g0336 |
3 | NA18956.hp2 NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1582-884G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735013 | |||||||
| chr11:47735016 | C | T | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1582-887G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735016 | |||||||
| chr11:47735150 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1582-1021T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735150 | |||||||
| chr11:47735299 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(9): Show |
12 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1582-1170T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735299 | |||||||
| chr11:47735429 | A | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1581+1187T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735429 | |||||||
| chr11:47735802 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1581+814G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735802 | |||||||
| chr11:47735816 | A | T | 1 | a0002c0003t0001g0263 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1581+800T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735816 | |||||||
| chr11:47735827 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0204 |
2 | NA18941.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1581+789G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735827 | |||||||
| chr11:47735842 | G | T | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1581+774C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735842 | |||||||
| chr11:47735895 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1581+721G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47735895 | |||||||
| chr11:47736078 | AC | A | 109 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1581+537delG | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736078 | |||||||
| chr11:47736079 | C | T | 1 | a0002c0002t0001g0336 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1581+537G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736079 | |||||||
| chr11:47736079 | CA | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1581+536delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736079 | |||||||
| chr11:47736080 | A | T | 109 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1581+536T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736080 | |||||||
| chr11:47736081 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1581+535T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736081 | |||||||
| chr11:47736149 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1581+467C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736149 | |||||||
| chr11:47736188 | C | A | 1 | a0002c0002t0001g0329 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1581+428G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736188 | |||||||
| chr11:47736195 | C | T | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1581+421G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736195 | |||||||
| chr11:47736244 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1581+372T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736244 | |||||||
| chr11:47736253 | G | A | 2 | a0002c0002t0001g0279 a0003c0004t0001g0337 |
2 | NA18979.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1581+363C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736253 | |||||||
| chr11:47736253 | G | GA | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1581+362dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736253 | |||||||
| chr11:47736253 | G | GAA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(90): Show |
96 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1581+361_1581+362d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736253 | |||||||
| chr11:47736342 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(10): Show |
13 | HG01123.hp1 HG02486.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1581+274G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736342 | |||||||
| chr11:47736359 | C | T | 3 | a0001c0001t0001g0083 a0001c0007t0001g0004 a0001c0007t0001g0005 |
3 | HG02896.hp2 HG02897.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1581+257G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736359 | |||||||
| chr11:47736462 | A | T | 1 | a0001c0001t0001g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1581+154T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736462 | |||||||
| chr11:47736488 | A | G | 1 | a0008c0012t0001g0197 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1581+128T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736488 | |||||||
| chr11:47736600 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(90): Show |
96 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1581+16A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 9/16 | chr11 | 47736600 | |||||||
| chr11:47736753 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0217 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1457-13G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736753 | |||||||
| chr11:47736755 | T | C | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1457-15A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736755 | |||||||
| chr11:47736811 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1457-71A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736811 | |||||||
| chr11:47736885 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1457-145T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736885 | |||||||
| chr11:47736897 | T | C | 83 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1457-157A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736897 | |||||||
| chr11:47736901 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0013 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1457-161A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736901 | |||||||
| chr11:47736979 | A | G | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1457-239T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736979 | |||||||
| chr11:47736980 | A | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1457-240T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47736980 | |||||||
| chr11:47737047 | C | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0121 |
3 | HG00140.hp1 HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1457-307G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737047 | |||||||
| chr11:47737123 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1457-383C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737123 | |||||||
| chr11:47737139 | C | T | 1 | a0010c0016t0001g0095 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1457-399G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737139 | |||||||
| chr11:47737184 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1457-444G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737184 | |||||||
| chr11:47737280 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0056 others(23): Show |
27 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1457-540G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737280 | |||||||
| chr11:47737284 | T | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1457-544A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737284 | |||||||
| chr11:47737445 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1457-705A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737445 | |||||||
| chr11:47737593 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0082 a0001c0001t0001g0094 others(3): Show |
6 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1457-853G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737593 | |||||||
| chr11:47737701 | A | G | 1 | a0002c0002t0001g0321 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1457-961T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737701 | |||||||
| chr11:47737733 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1457-993G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737733 | |||||||
| chr11:47737819 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1457-1079A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737819 | |||||||
| chr11:47737965 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1457-1225G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737965 | |||||||
| chr11:47737989 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(90): Show |
96 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1457-1249G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47737989 | |||||||
| chr11:47738038 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0047 others(64): Show |
69 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1457-1298G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738038 | |||||||
| chr11:47738069 | T | C | 1 | a0002c0002t0001g0280 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1457-1329A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738069 | |||||||
| chr11:47738254 | C | G | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0264 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1457-1514G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738254 | |||||||
| chr11:47738289 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1457-1549C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738289 | |||||||
| chr11:47738526 | T | C | 81 | a0001c0001t0001g0159 a0002c0002t0001g0235 a0002c0002t0001g0266 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1457-1786A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738526 | |||||||
| chr11:47738800 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1457-2060G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738800 | |||||||
| chr11:47738847 | A | AT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(13): Show |
16 | HG01978.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1457-2108dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(10): Show |
13 | HG00621.hp1 HG00621.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1457-2109_1457-210 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTT | 13 | a0001c0001t0001g0018 a0002c0002t0001g0264 a0002c0002t0001g0270 others(10): Show |
13 | HG00099.hp2 HG00438.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1457-2110_1457-210 others(7): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTT | 18 | a0001c0001t0001g0009 a0002c0002t0001g0235 a0002c0002t0001g0244 others(15): Show |
18 | HG00639.hp1 HG01071.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1457-2111_1457-210 others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTT | 6 | a0002c0002t0001g0254 a0002c0002t0001g0276 a0002c0002t0001g0287 others(3): Show |
6 | HG00280.hp2 HG00609.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1457-2112_1457-210 others(9): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTT | 6 | a0002c0002t0001g0237 a0002c0002t0001g0269 a0002c0002t0001g0281 others(3): Show |
6 | HG02738.hp2 HG02896.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1457-2113_1457-210 others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(3): Show |
10 | a0002c0002t0001g0292 a0002c0002t0001g0308 a0002c0002t0001g0309 others(7): Show |
10 | HG00408.hp1 HG00673.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1457-2117_1457-210 others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(4): Show |
2 | a0003c0004t0001g0339 a0003c0004t0001g0344 |
2 | HG02083.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1457-2118_1457-210 others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(5): Show |
1 | a0002c0002t0001g0333 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1457-2119_1457-210 others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(6): Show |
1 | a0003c0004t0001g0341 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1457-2120_1457-210 others(17): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0001g0325 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1457-2122_1457-210 others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(9): Show |
3 | a0002c0002t0001g0240 a0002c0002t0001g0307 a0002c0003t0001g0243 |
3 | HG01081.hp1 HG02523.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1457-2123_1457-210 others(20): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(10): Show |
2 | a0002c0002t0001g0236 a0002c0003t0001g0246 |
2 | HG01167.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1457-2124_1457-210 others(21): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(11): Show |
1 | a0002c0003t0001g0263 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1457-2125_1457-210 others(22): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | A | ATTTTTTT others(17): Show |
1 | a0002c0003t0001g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1457-2131_1457-210 others(28): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0001g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1457-2117_1457-210 others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(4): Show |
A | 3 | a0001c0007t0001g0004 a0001c0007t0001g0005 a0002c0020t0001g0262 |
3 | HG02896.hp2 HG02897.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1457-2118_1457-210 others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(7): Show |
A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
4 | HG01169.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1457-2121_1457-210 others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(8): Show |
A | 1 | a0002c0002t0001g0324 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1457-2122_1457-210 others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(11): Show |
A | 1 | a0002c0003t0001g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1457-2125_1457-210 others(22): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(12): Show |
A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0104 a0001c0001t0001g0131 others(2): Show |
5 | HG02056.hp1 HG02257.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1457-2126_1457-210 others(23): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(13): Show |
A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1457-2127_1457-210 others(24): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(14): Show |
A | 3 | a0001c0001t0001g0180 a0002c0002t0001g0322 a0004c0008t0001g0034 |
3 | HG02683.hp1 HG03098.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1457-2128_1457-210 others(25): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738847 | ATTTTTTT others(17): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1457-2131_1457-210 others(28): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738847 | |||||||
| chr11:47738969 | C | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1457-2229G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47738969 | |||||||
| chr11:47739051 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0068 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1457-2311A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739051 | |||||||
| chr11:47739107 | T | A | 1 | a0002c0002t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1457-2367A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739107 | |||||||
| chr11:47739216 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1457-2476A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739216 | |||||||
| chr11:47739226 | G | A | 1 | a0004c0008t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1457-2486C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739226 | |||||||
| chr11:47739258 | A | T | 7 | a0002c0002t0001g0276 a0002c0002t0001g0301 a0002c0002t0001g0316 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1457-2518T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739258 | |||||||
| chr11:47739537 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1457-2797A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739537 | |||||||
| chr11:47739658 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0065 others(9): Show |
12 | HG02523.hp2 NA18982.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.1457-2918G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739658 | |||||||
| chr11:47739690 | C | T | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1457-2950G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739690 | |||||||
| chr11:47739732 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1457-2992A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739732 | |||||||
| chr11:47739903 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1457-3163G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739903 | |||||||
| chr11:47739919 | C | T | 83 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1457-3179G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739919 | |||||||
| chr11:47739956 | TTTTG | T | 3 | a0002c0002t0001g0287 a0002c0002t0001g0295 a0002c0002t0001g0320 |
3 | HG00609.hp1 NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1457-3220_1457-321 others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739956 | |||||||
| chr11:47739956 | TTTTGTTT others(1): Show |
T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1457-3224_1457-321 others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47739956 | |||||||
| chr11:47740046 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1457-3306A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740046 | |||||||
| chr11:47740072 | T | TTA | 3 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0126 |
3 | NA18940.hp1 NA18941.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1457-3334_1457-333 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740072 | |||||||
| chr11:47740141 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1457-3401C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740141 | |||||||
| chr11:47740189 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1457-3449G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740189 | |||||||
| chr11:47740209 | G | A | 4 | a0002c0002t0001g0267 a0002c0002t0001g0268 a0002c0002t0001g0277 others(1): Show |
4 | HG01071.hp1 HG03017.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1457-3469C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740209 | |||||||
| chr11:47740285 | TGCGCCTG others(1394): Show |
T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456+2267_1457-354 others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740285 | |||||||
| chr11:47740388 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0152 |
2 | NA18989.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1456+3565C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740388 | |||||||
| chr11:47740425 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1456+3528T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740425 | |||||||
| chr11:47740440 | TTAAAA | T | 8 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0214 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1456+3508_1456+351 others(9): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740440 | |||||||
| chr11:47740599 | GT | G | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1456+3353delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740599 | |||||||
| chr11:47740632 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1456+3321G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740632 | |||||||
| chr11:47740633 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1456+3320C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740633 | |||||||
| chr11:47740747 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1456+3206G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47740747 | |||||||
| chr11:47741021 | C | T | 1 | a0002c0002t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1456+2932G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741021 | |||||||
| chr11:47741052 | A | G | 1 | a0002c0002t0001g0316 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1456+2901T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741052 | |||||||
| chr11:47741359 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1456+2594T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741359 | |||||||
| chr11:47741447 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1456+2506A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741447 | |||||||
| chr11:47741464 | T | C | 85 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1456+2489A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741464 | |||||||
| chr11:47741555 | C | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0130 others(3): Show |
6 | HG00609.hp2 NA18964.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456+2398G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741555 | |||||||
| chr11:47741705 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1456+2248T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741705 | |||||||
| chr11:47741708 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0217 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1456+2245G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741708 | |||||||
| chr11:47741713 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1456+2240C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741713 | |||||||
| chr11:47741754 | T | A | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1456+2199A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741754 | |||||||
| chr11:47741756 | C | CA | 3 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 |
3 | HG01175.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1456+2196dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741756 | |||||||
| chr11:47741778 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(9): Show |
12 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1456+2175C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741778 | |||||||
| chr11:47741814 | C | CA | 246 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1456+2138dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741814 | |||||||
| chr11:47741814 | C | CAA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(91): Show |
97 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1456+2137_1456+213 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741814 | |||||||
| chr11:47741824 | T | A | 2 | a0002c0002t0001g0235 a0002c0002t0001g0327 |
2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1456+2129A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741824 | |||||||
| chr11:47741858 | G | A | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1456+2095C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741858 | |||||||
| chr11:47741869 | T | G | 4 | a0002c0002t0001g0267 a0002c0002t0001g0268 a0002c0002t0001g0277 others(1): Show |
4 | HG01071.hp1 HG03017.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456+2084A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741869 | |||||||
| chr11:47741957 | A | G | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1456+1996T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741957 | |||||||
| chr11:47741981 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1456+1972G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47741981 | |||||||
| chr11:47742059 | C | G | 1 | a0002c0002t0001g0288 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1456+1894G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742059 | |||||||
| chr11:47742200 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0251 |
2 | HG01123.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1456+1753G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742200 | |||||||
| chr11:47742306 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1456+1647G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742306 | |||||||
| chr11:47742433 | G | A | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1456+1520C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742433 | |||||||
| chr11:47742477 | C | CA | 56 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0031 others(53): Show |
57 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1456+1475dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAA | 26 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0063 others(23): Show |
26 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.1456+1474_1456+147 others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA | 9 | a0002c0002t0001g0240 a0002c0002t0001g0250 a0002c0002t0001g0251 others(6): Show |
9 | HG00323.hp1 HG00438.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456+1469_1456+147 others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(1): Show |
9 | a0002c0002t0001g0238 a0002c0003t0001g0239 a0002c0003t0001g0241 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456+1468_1456+147 others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(2): Show |
6 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0269 others(3): Show |
6 | HG00438.hp2 HG01175.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456+1467_1456+147 others(13): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(3): Show |
20 | a0002c0002t0001g0245 a0002c0002t0001g0248 a0002c0002t0001g0254 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.1456+1466_1456+147 others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(4): Show |
29 | a0002c0002t0001g0235 a0002c0002t0001g0244 a0002c0002t0001g0247 others(26): Show |
29 | HG00673.hp1 HG00735.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1456+1465_1456+147 others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(5): Show |
21 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0271 others(18): Show |
21 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1456+1464_1456+147 others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(6): Show |
10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0002c0002t0001g0268 others(7): Show |
10 | HG01071.hp1 HG01433.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1456+1463_1456+147 others(17): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(7): Show |
4 | a0002c0002t0001g0275 a0002c0002t0001g0287 a0002c0002t0001g0336 others(1): Show |
4 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456+1462_1456+147 others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1456+1459_1456+147 others(21): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1456+1457_1456+147 others(23): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1456+1455_1456+147 others(25): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 |
3 | HG02630.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1456+1453_1456+147 others(27): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1456+1452_1456+147 others(28): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(19): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0016 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1456+1450_1456+147 others(30): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1456+1475_1456+147 others(42): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | CA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0020 others(60): Show |
66 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1456+1475delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742477 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1456+1466_1456+147 others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742477 | |||||||
| chr11:47742742 | T | C | 1 | a0002c0003t0001g0239 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1456+1211A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742742 | |||||||
| chr11:47742934 | GTCTT | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1456+1015_1456+101 others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47742934 | |||||||
| chr11:47743122 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0108 a0001c0001t0001g0114 others(1): Show |
4 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456+831A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743122 | |||||||
| chr11:47743346 | G | A | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1456+607C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743346 | |||||||
| chr11:47743354 | G | A | 3 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 |
3 | HG01175.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1456+599C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743354 | |||||||
| chr11:47743356 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1456+597T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743356 | |||||||
| chr11:47743589 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1456+364C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743589 | |||||||
| chr11:47743740 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456+213T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | 47743740 | |||||||
| chr11:47744324 | A | G | 1 | a0002c0002t0001g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1246-161T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47744324 | |||||||
| chr11:47744420 | CAT | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1246-259_1246-258d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47744420 | |||||||
| chr11:47744560 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(9): Show |
12 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1246-397G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47744560 | |||||||
| chr11:47744872 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1246-709A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47744872 | |||||||
| chr11:47745316 | G | A | 2 | a0004c0008t0001g0034 a0004c0008t0001g0035 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1245+740C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745316 | |||||||
| chr11:47745436 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1245+620C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745436 | |||||||
| chr11:47745481 | G | C | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1245+575C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745481 | |||||||
| chr11:47745571 | A | G | 2 | a0002c0002t0001g0266 a0002c0002t0001g0274 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1245+485T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745571 | |||||||
| chr11:47745676 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1245+380A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745676 | |||||||
| chr11:47745748 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1245+308G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745748 | |||||||
| chr11:47745852 | C | T | 1 | a0002c0020t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1245+204G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47745852 | |||||||
| chr11:47746006 | A | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1245+50T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 7/16 | chr11 | 47746006 | |||||||
| chr11:47746519 | C | CT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0051 others(6): Show |
9 | HG00609.hp2 HG02056.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.907-126dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47746519 | |||||||
| chr11:47746660 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG00280.hp1 HG02698.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-266C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47746660 | |||||||
| chr11:47746663 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG01109.hp1 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-269G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47746663 | |||||||
| chr11:47746716 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.907-322A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47746716 | |||||||
| chr11:47746825 | C | G | 1 | a0002c0002t0001g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.907-431G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47746825 | |||||||
| chr11:47747145 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.907-751G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747145 | |||||||
| chr11:47747173 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.907-779C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747173 | |||||||
| chr11:47747228 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0069 others(18): Show |
23 | HG00544.hp2 HG02083.hp1 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.907-834C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747228 | |||||||
| chr11:47747237 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0188 a0001c0001t0001g0193 |
3 | HG01261.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.907-843G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747237 | |||||||
| chr11:47747499 | G | A | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.907-1105C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747499 | |||||||
| chr11:47747565 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.907-1171G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747565 | |||||||
| chr11:47747575 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.907-1181C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747575 | |||||||
| chr11:47747672 | G | A | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.907-1278C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747672 | |||||||
| chr11:47747923 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.907-1529C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47747923 | |||||||
| chr11:47748012 | G | A | 79 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(76): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.907-1618C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748012 | |||||||
| chr11:47748068 | C | T | 60 | a0002c0002t0001g0235 a0002c0002t0001g0267 a0002c0002t0001g0268 others(57): Show |
60 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.907-1674G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748068 | |||||||
| chr11:47748070 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0061 others(10): Show |
13 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-1676C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748070 | |||||||
| chr11:47748106 | A | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.907-1712T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748106 | |||||||
| chr11:47748215 | G | A | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.907-1821C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748215 | |||||||
| chr11:47748384 | A | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.907-1990T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748384 | |||||||
| chr11:47748623 | C | T | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.907-2229G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748623 | |||||||
| chr11:47748624 | C | G | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.907-2230G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748624 | |||||||
| chr11:47748712 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02723.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.906+2204G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748712 | |||||||
| chr11:47748748 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0217 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+2168G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748748 | |||||||
| chr11:47748836 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.906+2080C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47748836 | |||||||
| chr11:47749096 | A | AAAAC | 157 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0036 others(154): Show |
159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.906+1816_906+1819d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749096 | |||||||
| chr11:47749096 | AAAAC | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0210 a0002c0002t0001g0303 others(1): Show |
4 | HG01167.hp2 HG01258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1816_906+1819d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749096 | |||||||
| chr11:47749324 | C | CACTTTGG others(2): Show |
332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.906+1591_906+1592i others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749324 | |||||||
| chr11:47749391 | G | A | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.906+1525C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749391 | |||||||
| chr11:47749427 | G | A | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.906+1489C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749427 | |||||||
| chr11:47749924 | T | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.906+992A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749924 | |||||||
| chr11:47749957 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.906+959C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47749957 | |||||||
| chr11:47750131 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.906+785G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750131 | |||||||
| chr11:47750157 | TC | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0203 |
3 | HG02148.hp2 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.906+758delG | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750157 | |||||||
| chr11:47750205 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.906+711G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750205 | |||||||
| chr11:47750381 | C | CA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(8): Show |
12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+534dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAA | 92 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0058 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.906+533_906+534dup others(2): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(93): Show |
99 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.906+532_906+534dup others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAAA | 37 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0048 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.906+531_906+534dup others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAAAA | 36 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0040 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.906+530_906+534dup others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAAAAA | 24 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0043 others(21): Show |
24 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.906+529_906+534dup others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAAAAAA | 13 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0072 others(10): Show |
13 | HG00140.hp1 HG00735.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+528_906+534dup others(7): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0096 others(3): Show |
6 | HG01175.hp1 HG03654.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+527_906+534dup others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | CA | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(11): Show |
14 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.906+534delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750381 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.906+522_906+534del others(13): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750381 | |||||||
| chr11:47750450 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.906+466C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750450 | |||||||
| chr11:47750577 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.906+339C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750577 | |||||||
| chr11:47750656 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.906+260A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750656 | |||||||
| chr11:47750684 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0206 |
2 | NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.906+232C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750684 | |||||||
| chr11:47750688 | CAA | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(17): Show |
20 | HG00280.hp1 HG01978.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.906+226_906+227del others(2): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750688 | CAAA | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(37): Show |
40 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.906+225_906+227del others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750688 | CAAAA | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0029 others(127): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.906+224_906+227del others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750688 | CAAAAA | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0204 a0002c0002t0001g0238 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.906+223_906+227del others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750688 | CAAAAAA | C | 101 | a0001c0001t0001g0074 a0002c0002t0001g0235 a0002c0002t0001g0236 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.906+222_906+227del others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750688 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0226 |
2 | HG03704.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.906+217_906+227del others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750688 | |||||||
| chr11:47750706 | AAAAAAAA others(5): Show |
A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0210 a0001c0001t0001g0214 others(5): Show |
8 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.906+198_906+209del others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750706 | |||||||
| chr11:47750707 | AAAAAAAA others(4): Show |
A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0058 others(18): Show |
22 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.906+198_906+208del others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750707 | |||||||
| chr11:47750708 | AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0150 a0001c0001t0001g0212 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+198_906+207del others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750708 | |||||||
| chr11:47750796 | G | C | 1 | a0002c0002t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.906+120C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750796 | |||||||
| chr11:47750849 | C | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.906+67G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750849 | |||||||
| chr11:47750906 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+10G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 6/16 | chr11 | 47750906 | |||||||
| chr11:47751352 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.638-62G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751352 | |||||||
| chr11:47751373 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-83T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751373 | |||||||
| chr11:47751411 | G | C | 24 | a0002c0002t0001g0237 a0002c0002t0001g0244 a0002c0002t0001g0245 others(21): Show |
24 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.638-121C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751411 | |||||||
| chr11:47751655 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0031 others(93): Show |
99 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.638-365A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751655 | |||||||
| chr11:47751674 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
132 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.638-384G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751674 | |||||||
| chr11:47751688 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.638-398G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751688 | |||||||
| chr11:47751780 | T | C | 5 | a0002c0003t0001g0249 a0002c0003t0001g0256 a0002c0003t0001g0257 others(2): Show |
5 | HG00323.hp1 HG01496.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-490A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751780 | |||||||
| chr11:47751966 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.638-676T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47751966 | |||||||
| chr11:47752373 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+543G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752373 | |||||||
| chr11:47752425 | CA | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0029 others(171): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.637+490delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752425 | |||||||
| chr11:47752425 | CAA | C | 108 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+489_637+490del others(2): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752425 | |||||||
| chr11:47752686 | C | T | 80 | a0002c0002t0001g0235 a0002c0002t0001g0266 a0002c0002t0001g0267 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.637+230G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752686 | |||||||
| chr11:47752814 | A | AAAAC | 85 | a0001c0001t0001g0003 a0001c0001t0001g0166 a0001c0001t0001g0186 others(82): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.637+98_637+101dupG others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752814 | |||||||
| chr11:47752884 | C | T | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0264 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637+32G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 4/16 | chr11 | 47752884 | |||||||
| chr11:47753272 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0065 others(9): Show |
12 | HG02523.hp2 NA18982.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-170G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753272 | |||||||
| chr11:47753302 | T | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.451-200A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753302 | |||||||
| chr11:47753543 | G | A | 1 | a0001c0015t0001g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451-441C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753543 | |||||||
| chr11:47753619 | C | A | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.451-517G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753619 | |||||||
| chr11:47753645 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.451-543A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753645 | |||||||
| chr11:47753759 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.451-657T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47753759 | |||||||
| chr11:47754009 | A | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.450+519T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754009 | |||||||
| chr11:47754101 | T | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.450+427A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754101 | |||||||
| chr11:47754132 | C | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+396G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754132 | |||||||
| chr11:47754209 | GAAA | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+316_450+318del others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754209 | |||||||
| chr11:47754391 | G | A | 1 | a0002c0002t0001g0330 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.450+137C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754391 | |||||||
| chr11:47754399 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0025 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.450+129G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754399 | |||||||
| chr11:47754400 | A | G | 7 | a0002c0002t0001g0276 a0002c0002t0001g0301 a0002c0002t0001g0316 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+128T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 3/16 | chr11 | 47754400 | |||||||
| chr11:47754731 | C | T | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-67G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47754731 | |||||||
| chr11:47754911 | G | A | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0264 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.314-247C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47754911 | |||||||
| chr11:47754991 | A | C | 1 | a0002c0003t0001g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.314-327T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47754991 | |||||||
| chr11:47755134 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.314-470G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755134 | |||||||
| chr11:47755141 | T | TA | 6 | a0001c0001t0001g0086 a0001c0001t0001g0120 a0002c0002t0001g0279 others(3): Show |
6 | HG00735.hp1 HG03098.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-478dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755141 | |||||||
| chr11:47755141 | TA | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(110): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.314-478delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755141 | |||||||
| chr11:47755411 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.314-747A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755411 | |||||||
| chr11:47755635 | C | CA | 42 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0054 others(39): Show |
43 | HG01109.hp1 HG01243.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.314-972dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755635 | |||||||
| chr11:47755635 | CA | C | 116 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0025 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.314-972delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755635 | |||||||
| chr11:47755649 | A | G | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-985T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755649 | |||||||
| chr11:47755652 | G | A | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-988C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755652 | |||||||
| chr11:47755656 | A | G | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-992T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755656 | |||||||
| chr11:47755666 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0151 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-1002T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755666 | |||||||
| chr11:47755685 | T | A | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-1021A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755685 | |||||||
| chr11:47755919 | A | C | 1 | a0008c0012t0001g0197 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.314-1255T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47755919 | |||||||
| chr11:47756066 | G | C | 1 | a0002c0020t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.314-1402C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756066 | |||||||
| chr11:47756134 | T | C | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.314-1470A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756134 | |||||||
| chr11:47756207 | T | C | 1 | a0002c0006t0001g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.314-1543A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756207 | |||||||
| chr11:47756213 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314-1549G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756213 | |||||||
| chr11:47756368 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.314-1704C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756368 | |||||||
| chr11:47756393 | T | A | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-1729A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756393 | |||||||
| chr11:47756447 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.314-1783T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756447 | |||||||
| chr11:47756475 | A | G | 1 | a0001c0005t0001g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-1811T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756475 | |||||||
| chr11:47756546 | TTTG | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02809.hp2 HG02897.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-1885_314-1883d others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756546 | |||||||
| chr11:47756556 | T | C | 1 | a0002c0002t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.314-1892A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756556 | |||||||
| chr11:47756573 | C | T | 7 | a0002c0002t0001g0276 a0002c0002t0001g0301 a0002c0002t0001g0316 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-1909G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756573 | |||||||
| chr11:47756694 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0180 |
2 | NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.314-2030G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756694 | |||||||
| chr11:47756705 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-2041G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756705 | |||||||
| chr11:47756956 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.314-2292G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756956 | |||||||
| chr11:47756977 | C | G | 20 | a0002c0002t0001g0266 a0002c0002t0001g0271 a0002c0002t0001g0272 others(17): Show |
20 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.314-2313G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47756977 | |||||||
| chr11:47757073 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0122 a0001c0001t0001g0209 |
3 | HG00597.hp2 NA18962.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.314-2409C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757073 | |||||||
| chr11:47757194 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314-2530G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757194 | |||||||
| chr11:47757225 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0031 others(94): Show |
100 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.314-2561T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757225 | |||||||
| chr11:47757373 | G | A | 1 | a0002c0002t0001g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.314-2709C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757373 | |||||||
| chr11:47757455 | G | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0123 others(4): Show |
7 | NA18747.hp1 NA18990.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-2791C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757455 | |||||||
| chr11:47757487 | T | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.314-2823A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757487 | |||||||
| chr11:47757493 | T | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-2829A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757493 | |||||||
| chr11:47757589 | G | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.314-2925C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757589 | |||||||
| chr11:47757737 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.314-3073C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757737 | |||||||
| chr11:47757832 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.314-3168A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757832 | |||||||
| chr11:47757833 | A | ATATG | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-3173_314-3170d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757833 | |||||||
| chr11:47757847 | C | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.314-3183G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757847 | |||||||
| chr11:47757918 | T | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0031 others(94): Show |
100 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.314-3254A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757918 | |||||||
| chr11:47757951 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0126 |
3 | NA18940.hp1 NA18941.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.314-3287A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47757951 | |||||||
| chr11:47758034 | C | T | 80 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0033 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.314-3370G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758034 | |||||||
| chr11:47758264 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.314-3600G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758264 | |||||||
| chr11:47758494 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314-3830C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758494 | |||||||
| chr11:47758528 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.314-3864G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758528 | |||||||
| chr11:47758583 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.314-3919C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758583 | |||||||
| chr11:47758607 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-3943C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758607 | |||||||
| chr11:47758649 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.314-3985C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758649 | |||||||
| chr11:47758670 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.314-4006C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758670 | |||||||
| chr11:47758837 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.314-4173C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758837 | |||||||
| chr11:47758852 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314-4188G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758852 | |||||||
| chr11:47758864 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.314-4200T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758864 | |||||||
| chr11:47758867 | G | C | 1 | a0001c0015t0001g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.314-4203C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758867 | |||||||
| chr11:47758878 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.314-4214C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758878 | |||||||
| chr11:47758899 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.314-4235C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758899 | |||||||
| chr11:47758920 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0032 others(87): Show |
93 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-4257dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758920 | |||||||
| chr11:47758938 | AG | A | 11 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0210 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-4275delC | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47758938 | |||||||
| chr11:47759076 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314-4412G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759076 | |||||||
| chr11:47759117 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.314-4453T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759117 | |||||||
| chr11:47759202 | G | T | 80 | a0002c0002t0001g0235 a0002c0002t0001g0266 a0002c0002t0001g0267 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.314-4538C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759202 | |||||||
| chr11:47759217 | CT | C | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.314-4554delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759217 | |||||||
| chr11:47759505 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.314-4841G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759505 | |||||||
| chr11:47759510 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.314-4846C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759510 | |||||||
| chr11:47759754 | A | G | 79 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0033 others(76): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.314-5090T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759754 | |||||||
| chr11:47759908 | G | T | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-5244C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759908 | |||||||
| chr11:47759982 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.313+5288A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47759982 | |||||||
| chr11:47760192 | A | T | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.313+5078T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760192 | |||||||
| chr11:47760207 | T | C | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.313+5063A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760207 | |||||||
| chr11:47760232 | CAG | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+5036_313+5037d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760232 | |||||||
| chr11:47760258 | CATT | C | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0003t0001g0260 |
3 | HG02004.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.313+5009_313+5011d others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760258 | |||||||
| chr11:47760259 | A | AT | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0076 others(9): Show |
12 | HG01109.hp1 NA18940.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+5010dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760259 | |||||||
| chr11:47760259 | AT | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
31 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.313+5010delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760259 | |||||||
| chr11:47760259 | ATT | A | 99 | a0001c0001t0001g0013 a0002c0002t0001g0235 a0002c0002t0001g0236 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.313+5009_313+5010d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760259 | |||||||
| chr11:47760313 | A | G | 30 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.313+4957T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760313 | |||||||
| chr11:47760409 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.313+4861C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760409 | |||||||
| chr11:47760436 | G | GT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0093 others(10): Show |
13 | HG00323.hp1 HG00438.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+4833dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760436 | |||||||
| chr11:47760436 | GT | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0031 others(93): Show |
99 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.313+4833delA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760436 | |||||||
| chr11:47760451 | G | T | 1 | a0002c0002t0001g0334 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.313+4819C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760451 | |||||||
| chr11:47760484 | C | T | 2 | a0002c0002t0001g0334 a0002c0002t0001g0335 |
2 | NA18956.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.313+4786G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760484 | |||||||
| chr11:47760524 | C | T | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+4746G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760524 | |||||||
| chr11:47760645 | G | A | 4 | a0002c0002t0001g0272 a0002c0002t0001g0288 a0002c0002t0001g0323 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+4625C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47760645 | |||||||
| chr11:47761051 | C | T | 1 | a0005c0014t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.313+4219G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761051 | |||||||
| chr11:47761078 | T | A | 2 | a0001c0007t0001g0004 a0001c0007t0001g0005 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.313+4192A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761078 | |||||||
| chr11:47761188 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.313+4082G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761188 | |||||||
| chr11:47761242 | A | G | 1 | a0002c0002t0001g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.313+4028T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761242 | |||||||
| chr11:47761483 | T | A | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.313+3787A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761483 | |||||||
| chr11:47761524 | G | A | 81 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0033 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.313+3746C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761524 | |||||||
| chr11:47761596 | CA | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.313+3673delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761596 | |||||||
| chr11:47761677 | G | T | 31 | a0002c0002t0001g0235 a0002c0002t0001g0270 a0002c0002t0001g0279 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.313+3593C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761677 | |||||||
| chr11:47761835 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+3435A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47761835 | |||||||
| chr11:47762030 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.313+3240C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762030 | |||||||
| chr11:47762052 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0214 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+3218C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762052 | |||||||
| chr11:47762062 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.313+3208A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762062 | |||||||
| chr11:47762096 | C | G | 9 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0126 others(6): Show |
9 | HG03942.hp2 NA18940.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+3174G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762096 | |||||||
| chr11:47762138 | G | GT | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.313+3131dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762138 | |||||||
| chr11:47762196 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0212 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.313+3074C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762196 | |||||||
| chr11:47762374 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0204 |
2 | NA18941.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.313+2896C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762374 | |||||||
| chr11:47762414 | A | T | 1 | a0009c0017t0001g0128 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.313+2856T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762414 | |||||||
| chr11:47762637 | G | C | 11 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0210 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+2633C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762637 | |||||||
| chr11:47762906 | C | CA | 14 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.313+2363dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47762906 | C | CAAA | 74 | a0002c0002t0001g0264 a0002c0002t0001g0267 a0002c0002t0001g0269 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.313+2361_313+2363d others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47762906 | C | CAAAA | 31 | a0002c0002t0001g0235 a0002c0002t0001g0237 a0002c0002t0001g0244 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.313+2360_313+2363d others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47762906 | C | CAAAAAA | 61 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0037 others(58): Show |
61 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.313+2358_313+2363d others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47762906 | C | CAAAAAAA | 17 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(14): Show |
17 | HG00642.hp1 HG01175.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.313+2357_313+2363d others(9): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47762906 | CAAAAAAA others(2): Show |
C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
131 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.313+2355_313+2363d others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47762906 | |||||||
| chr11:47763082 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0214 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+2188C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763082 | |||||||
| chr11:47763088 | C | T | 1 | a0002c0002t0001g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.313+2182G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763088 | |||||||
| chr11:47763189 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.313+2081G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763189 | |||||||
| chr11:47763420 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG00597.hp1 HG01884.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.313+1849delT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763420 | |||||||
| chr11:47763420 | CAA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.313+1848_313+1849d others(4): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763420 | |||||||
| chr11:47763420 | CAAA | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0096 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.313+1847_313+1849d others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763420 | |||||||
| chr11:47763492 | GTGTTT | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.313+1773_313+1777d others(7): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763492 | |||||||
| chr11:47763514 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.313+1756C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763514 | |||||||
| chr11:47763733 | G | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+1537C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763733 | |||||||
| chr11:47763752 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.313+1518C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763752 | |||||||
| chr11:47763763 | A | T | 1 | a0009c0017t0001g0128 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.313+1507T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763763 | |||||||
| chr11:47763795 | T | C | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+1475A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47763795 | |||||||
| chr11:47764107 | T | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0232 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+1163A>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764107 | |||||||
| chr11:47764361 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.313+909G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764361 | |||||||
| chr11:47764455 | A | T | 1 | a0009c0017t0001g0128 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.313+815T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764455 | |||||||
| chr11:47764525 | G | GT | 14 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0048 others(11): Show |
14 | HG00597.hp1 HG01175.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.313+744dupA | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764525 | |||||||
| chr11:47764570 | C | T | 1 | a0002c0002t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.313+700G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764570 | |||||||
| chr11:47764632 | C | T | 80 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0033 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.313+638G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764632 | |||||||
| chr11:47764649 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.313+621T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764649 | |||||||
| chr11:47764820 | G | C | 30 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.313+450C>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764820 | |||||||
| chr11:47764862 | A | G | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+408T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764862 | |||||||
| chr11:47764932 | G | T | 1 | a0002c0002t0001g0280 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.313+338C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764932 | |||||||
| chr11:47764939 | A | G | 2 | a0001c0010t0001g0345 a0001c0010t0001g0346 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.313+331T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764939 | |||||||
| chr11:47764973 | G | T | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.313+297C>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47764973 | |||||||
| chr11:47765036 | G | GA | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0210 others(6): Show |
9 | HG01169.hp2 HG01517.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.313+233dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 2/16 | chr11 | 47765036 | |||||||
| chr11:47765374 | A | AAAAAG | 104 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0064 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-17_221-13dupCT others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | A | AAAAAGAA others(3): Show |
74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
78 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.221-22_221-13dupCT others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | A | AAAAAGAA others(8): Show |
23 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0054 others(20): Show |
23 | HG01169.hp1 HG01358.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.221-27_221-13dupCT others(13): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | A | AAAAAGAA others(13): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
2 | HG00597.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.221-32_221-13dupCT others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | A | G | 3 | a0002c0002t0001g0247 a0002c0002t0001g0264 a0002c0002t0001g0296 |
3 | HG02965.hp1 HG03139.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.221-12T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | AAAAAG | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0194 others(6): Show |
9 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-17_221-13delCT others(3): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765374 | AAAAAGAA others(8): Show |
A | 4 | a0001c0001t0001g0008 a0001c0007t0001g0004 a0001c0007t0001g0005 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-27_221-13delCT others(13): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765374 | |||||||
| chr11:47765376 | A | AAAGAAAA others(1): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-22_221-15dupCT others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765376 | |||||||
| chr11:47765389 | G | GAAAAGAA others(9): Show |
1 | a0001c0001t0001g0133 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.221-43_221-28dupTC others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765389 | |||||||
| chr11:47765389 | G | GAAAAGAA others(14): Show |
1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.221-48_221-28dupTC others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765389 | |||||||
| chr11:47765401 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00741.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.221-39T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765401 | |||||||
| chr11:47765536 | C | T | 1 | a0002c0002t0001g0287 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.221-174G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765536 | |||||||
| chr11:47765567 | C | CCGGGGGG others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.221-206_221-205ins others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(1): Show |
20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0057 others(17): Show |
20 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.221-213_221-206dup others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(3): Show |
11 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0149 others(8): Show |
11 | HG01517.hp1 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-215_221-206dup others(10): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(4): Show |
15 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
15 | HG00408.hp2 HG01978.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.221-216_221-206dup others(11): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(5): Show |
10 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0140 others(7): Show |
10 | HG01175.hp2 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-217_221-206dup others(12): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(6): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0138 others(1): Show |
4 | HG01243.hp2 HG03669.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-218_221-206dup others(13): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(7): Show |
9 | a0001c0001t0001g0051 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-219_221-206dup others(14): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(8): Show |
4 | a0001c0001t0001g0050 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG00597.hp1 HG03492.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-220_221-206dup others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(9): Show |
3 | a0001c0001t0001g0049 a0002c0002t0001g0285 a0002c0003t0001g0241 |
3 | HG00642.hp2 NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.221-206_221-205ins others(16): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(10): Show |
2 | a0001c0001t0001g0048 a0002c0002t0001g0270 |
2 | NA18964.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.221-206_221-205ins others(17): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(11): Show |
2 | a0001c0001t0001g0047 a0002c0002t0001g0269 |
2 | HG02056.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.221-206_221-205ins others(18): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(12): Show |
2 | a0001c0001t0001g0032 a0002c0002t0001g0284 |
2 | HG04204.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.221-206_221-205ins others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(13): Show |
2 | a0001c0001t0001g0130 a0002c0002t0001g0268 |
2 | HG01071.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.221-206_221-205ins others(20): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(14): Show |
2 | a0002c0002t0001g0240 a0002c0002t0001g0283 |
2 | HG00438.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.221-206_221-205ins others(21): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(15): Show |
1 | a0002c0002t0001g0267 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-206_221-205ins others(22): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | C | CGGGGGGG others(68): Show |
1 | a0001c0001t0001g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.221-206_221-205ins others(75): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765567 | CG | C | 63 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0043 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.221-206delC | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765567 | |||||||
| chr11:47765568 | G | GA | 3 | a0001c0001t0001g0037 a0001c0001t0001g0064 a0001c0001t0001g0067 |
3 | HG02602.hp2 HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.221-207_221-206ins others(1): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765568 | |||||||
| chr11:47765569 | G | A | 28 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(25): Show |
28 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.221-207C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765569 | |||||||
| chr11:47765570 | G | A | 48 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0043 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.221-208C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765570 | |||||||
| chr11:47765574 | G | GGGGGGGG others(8): Show |
1 | a0002c0002t0001g0282 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.221-213_221-212ins others(15): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765574 | |||||||
| chr11:47765582 | GC | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0161 others(2): Show |
5 | HG02622.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-221delG | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765582 | |||||||
| chr11:47765583 | C | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00323.hp1 HG00609.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.221-221G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765583 | |||||||
| chr11:47765583 | C | T | 2 | a0002c0002t0001g0235 a0002c0002t0001g0327 |
2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.221-221G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765583 | |||||||
| chr11:47765606 | A | C | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.221-244T>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765606 | |||||||
| chr11:47765651 | A | AAAAAT | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.221-290_221-289ins others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765651 | |||||||
| chr11:47765851 | C | CTTTTT | 14 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(11): Show |
14 | HG01069.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-494_221-490dup others(5): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765851 | |||||||
| chr11:47765851 | C | CTTTTTT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
98 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.221-495_221-490dup others(6): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765851 | |||||||
| chr11:47765851 | C | CTTTTTTT | 171 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.221-496_221-490dup others(7): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765851 | |||||||
| chr11:47765851 | C | CTTTTTTT others(1): Show |
37 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(34): Show |
37 | HG00621.hp2 HG00741.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.221-497_221-490dup others(8): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765851 | |||||||
| chr11:47765851 | C | T | 1 | a0001c0011t0001g0224 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.221-489G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765851 | |||||||
| chr11:47765873 | G | A | 3 | a0002c0002t0001g0334 a0002c0002t0001g0335 a0002c0002t0001g0336 |
3 | NA18956.hp2 NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.221-511C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765873 | |||||||
| chr11:47765882 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.221-520A>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765882 | |||||||
| chr11:47765893 | G | A | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.221-531C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765893 | |||||||
| chr11:47765976 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.221-614C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765976 | |||||||
| chr11:47765986 | G | A | 110 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.221-624C>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47765986 | |||||||
| chr11:47766003 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.221-641T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766003 | |||||||
| chr11:47766119 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18943.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.221-757T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766119 | |||||||
| chr11:47766150 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.221-788G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766150 | |||||||
| chr11:47766315 | G | GA | 4 | a0001c0005t0001g0227 a0001c0005t0001g0228 a0001c0005t0001g0229 others(1): Show |
4 | HG03942.hp2 NA18952.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+753dupT | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766315 | |||||||
| chr11:47766325 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+744T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766325 | |||||||
| chr11:47766339 | A | T | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.220+730T>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766339 | |||||||
| chr11:47766464 | C | G | 1 | a0002c0002t0001g0266 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220+605G>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766464 | |||||||
| chr11:47766466 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.220+603A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766466 | |||||||
| chr11:47766511 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.220+558A>G | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766511 | |||||||
| chr11:47766772 | A | G | 30 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.220+297T>C | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766772 | |||||||
| chr11:47766853 | C | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG02257.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.220+216G>T | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766853 | |||||||
| chr11:47766938 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.220+131G>A | FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 1/16 | chr11 | 47766938 |