Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55325 |
| ensemblid | ENSG00000109775.11 |
| hgncid | 25640 |
| symbol | UFSP2 |
| name | UFM1 specific peptidase 2 |
| refseq_nuc | NM_018359.5 |
| refseq_prot | NP_060829.2 |
| ensembl_nuc | ENST00000264689.11 |
| ensembl_prot | ENSP00000264689.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 185399537 |
| end | 185425964 |
| strand | - |
| ver | v1.2 |
| region | chr4:185399537-185425964 |
| region5000 | chr4:185394537-185430964 |
| regionname0 | UFSP2_chr4_185399537_185425964 |
| regionname5000 | UFSP2_chr4_185394537_185430964 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 469 | 290 | 88 | 47 | 98 | 12 | 43 | 76 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0002 | 0/0 | 469 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0003 | 0/0 | 469 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0004 | 0/0 | 469 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0005 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0006 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0007 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| a0008 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | MVISE others(464): Show |
chr4 | 185394537 | 185430964 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1407 | 264 | 76 | 46 | 87 | 12 | 41 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0002 | 0/0 | 1407 | 16 | 3 | 1 | 10 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0004 | 0/0 | 1407 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0005 | 0/0 | 1407 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0006 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0008 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0001c0010 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0002c0003 | 0/0 | 1407 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0003c0007 | 0/0 | 1407 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0004c0011 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0005c0013 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0006c0014 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0007c0012 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 | ||
| a0008c0009 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | ATGGT others(1402): Show |
chr4 | 185394537 | 185430964 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2361 | 116 | 11 | 30 | 51 | 9 | 15 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0002 | 1/0 | 2361 | 50 | 22 | 13 | 4 | 2 | 8 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0003 | 0/0 | 2361 | 41 | 15 | 1 | 18 | 1 | 6 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0004 | 0/0 | 2361 | 18 | 3 | 0 | 12 | 0 | 3 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0005 | 0/0 | 2361 | 20 | 18 | 1 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0006 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0007 | 0/0 | 2361 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0008 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0009 | 0/0 | 2361 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0010 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0011 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0012 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0013 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0014 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0015 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0016 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0017 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0018 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0019 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0001t0020 | 0/1 | 2361 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0002t0004 | 0/0 | 2361 | 7 | 0 | 0 | 7 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0002t0006 | 0/0 | 2361 | 7 | 3 | 1 | 1 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0002t0007 | 0/0 | 2361 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0004t0002 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0005t0006 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0006t0005 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0008t0002 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0001c0010t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0002c0003t0002 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0003c0007t0005 | 0/0 | 2361 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0004c0011t0002 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0005c0013t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0006c0014t0001 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0007c0012t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| a0008c0009t0001 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | GCCCC others(2356): Show |
chr4 | 185394537 | 185430964 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 1 | 9 | 7 | 3 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0003 | 0/0 | 7 | 2 | 2 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0004 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0002 | 0/0 | 8 | 0 | 0 | 2 | 1 | 5 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0012g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0015g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0017g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0001t0020g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0002t0007g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0004t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0005t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0005t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0006t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0008t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0001c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0002c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0002c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0002c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0003c0007t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0003c0007t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0004c0011t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0005c0013t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0006c0014t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0007c0012t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| a0008c0009t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0127 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00639 | hp1 | a0001 | c0002 | t0006 | g0090 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00642 | hp2 | a0003 | c0007 | t0005 | g0100 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01081 | hp2 | a0004 | c0011 | t0002 | g0044 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01934 | hp1 | a0003 | c0007 | t0005 | g0103 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02015 | hp2 | a0005 | c0013 | t0001 | g0177 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02055 | hp1 | a0006 | c0014 | t0001 | g0190 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0075 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02083 | hp2 | a0007 | c0012 | t0001 | g0175 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0101 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02165 | hp2 | a0001 | c0002 | t0006 | g0105 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0102 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0077 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02572 | hp1 | a0001 | c0005 | t0006 | g0026 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02615 | hp2 | a0001 | c0005 | t0006 | g0026 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02735 | hp2 | a0008 | c0009 | t0001 | g0184 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0121 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02818 | hp1 | a0001 | c0006 | t0005 | g0030 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02970 | hp2 | a0002 | c0003 | t0002 | g0079 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0040 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0088 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0104 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03491 | hp1 | a0001 | c0002 | t0006 | g0089 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0084 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0193 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03579 | hp1 | a0001 | c0006 | t0005 | g0030 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03654 | hp1 | a0001 | c0002 | t0006 | g0091 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0196 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0046 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03834 | hp2 | a0001 | c0001 | t0012 | g0043 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0116 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0118 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0119 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0197 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18970 | hp2 | a0001 | c0001 | t0015 | g0123 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18973 | hp1 | a0001 | c0001 | t0017 | g0124 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18975 | hp1 | a0001 | c0010 | t0001 | g0140 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0129 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19064 | hp1 | a0001 | c0002 | t0004 | g0130 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19064 | hp2 | a0001 | c0002 | t0007 | g0032 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19083 | hp1 | a0001 | c0002 | t0007 | g0032 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ASW | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0107 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0085 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0110 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA20300 | hp2 | a0001 | c0001 | t0019 | g0133 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA21309 | hp1 | a0001 | c0008 | t0002 | g0067 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0020 | g0199 | REF | REF | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0025 | REF | REF | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185403591 | A | G | 1 | a0004 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1226T>C | p.Leu409Pro | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/12 | 1322/2361 | 1226/1410 | 409/469 | chr4 | 185403591 | |||
| chr4:185408335 | C | G | 1 | a0002 | 3 | HG02055.hp2 HG02451.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.932G>C | p.Cys311Ser | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/12 | 1028/2361 | 932/1410 | 311/469 | chr4 | 185408335 | |||
| chr4:185413748 | G | A | 1 | a0007 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.809C>T | p.Pro270Leu | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/12 | 905/2361 | 809/1410 | 270/469 | chr4 | 185413748 | |||
| chr4:185415221 | T | G | 1 | a0005 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.618A>C | p.Lys206Asn | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 714/2361 | 618/1410 | 206/469 | chr4 | 185415221 | |||
| chr4:185415276 | A | G | 1 | a0008 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.563T>C | p.Met188Thr | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 659/2361 | 563/1410 | 188/469 | chr4 | 185415276 | |||
| chr4:185418466 | T | C | 1 | a0003 | 2 | HG00642.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.308A>G | p.Lys103Arg | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/12 | 404/2361 | 308/1410 | 103/469 | chr4 | 185418466 | |||
| chr4:185418667 | T | C | 1 | a0006 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.186A>G | p.Ile62Met | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 282/2361 | 186/1410 | 62/469 | chr4 | 185418667 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185403521 | A | G | 1 | a0001c0004 | 3 | HG02145.hp1 HG02818.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1296T>C | p.Ala432Ala | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/12 | 1392/2361 | 1296/1410 | 432/469 | chr4 | 185403521 | |||
| chr4:185407965 | G | T | 1 | a0001c0010 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.1092C>A | p.Ile364Ile | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/12 | 1188/2361 | 1092/1410 | 364/469 | chr4 | 185407965 | |||
| chr4:185415311 | T | C | 2 | a0001c0002 a0001c0005 |
19 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(16): Show |
synonymous_variant | LOW | c.528A>G | p.Gln176Gln | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 624/2361 | 528/1410 | 176/469 | chr4 | 185415311 | |||
| chr4:185418495 | T | C | 1 | a0001c0005 | 3 | HG02486.hp1 HG02572.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.279A>G | p.Glu93Glu | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/12 | 375/2361 | 279/1410 | 93/469 | chr4 | 185418495 | |||
| chr4:185418616 | A | G | 1 | a0001c0006 | 2 | HG02818.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.237T>C | p.Ser79Ser | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 333/2361 | 237/1410 | 79/469 | chr4 | 185418616 | |||
| chr4:185418625 | A | G | 1 | a0001c0008 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.228T>C | p.Thr76Thr | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 324/2361 | 228/1410 | 76/469 | chr4 | 185418625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185399647 | C | A | 1 | a0001c0001t0013 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 745 | chr4 | 185399647 | ||||||
| chr4:185399726 | A | G | 3 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0019 |
43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*666T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 666 | chr4 | 185399726 | ||||||
| chr4:185399736 | G | A | 1 | a0001c0001t0009 | 2 | HG03017.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*656C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 656 | chr4 | 185399736 | ||||||
| chr4:185399752 | C | G | 3 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0019 |
43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 640 | chr4 | 185399752 | ||||||
| chr4:185399808 | G | A | 1 | a0001c0001t0008 | 2 | HG02145.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*584C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 584 | chr4 | 185399808 | ||||||
| chr4:185399816 | C | T | 1 | a0001c0001t0015 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 576 | chr4 | 185399816 | ||||||
| chr4:185399913 | C | T | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(15): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*479G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 479 | chr4 | 185399913 | ||||||
| chr4:185399927 | G | C | 1 | a0001c0001t0012 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 465 | chr4 | 185399927 | ||||||
| chr4:185399978 | A | T | 1 | a0001c0008t0002 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 414 | chr4 | 185399978 | ||||||
| chr4:185400055 | C | T | 1 | a0001c0001t0010 | 2 | HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*337G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 337 | chr4 | 185400055 | ||||||
| chr4:185400062 | T | C | 1 | a0001c0001t0017 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 330 | chr4 | 185400062 | ||||||
| chr4:185400128 | C | T | 6 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0014 others(3): Show |
28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 264 | chr4 | 185400128 | ||||||
| chr4:185400293 | C | G | 10 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(7): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 99 | chr4 | 185400293 | ||||||
| chr4:185400308 | A | G | 1 | a0001c0001t0014 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 84 | chr4 | 185400308 | ||||||
| chr4:185425886 | G | A | 1 | a0001c0001t0013 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 18 | chr4 | 185425886 | ||||||
| chr4:185425901 | G | A | 9 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(6): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 33 | chr4 | 185425901 | ||||||
| chr4:185425919 | G | C | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(14): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 51 | chr4 | 185425919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185400493 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1324-15G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400493 | |||||||
| chr4:185400635 | C | A | 1 | a0001c0001t0003g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1324-157G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400635 | |||||||
| chr4:185400662 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1324-184A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400662 | |||||||
| chr4:185400708 | A | G | 5 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0045 others(2): Show |
5 | HG01081.hp2 HG01433.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-230T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400708 | |||||||
| chr4:185400725 | T | A | 1 | a0001c0001t0002g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1324-247A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400725 | |||||||
| chr4:185400848 | G | T | 27 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1324-370C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400848 | |||||||
| chr4:185400880 | T | G | 1 | a0001c0001t0002g0023 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1324-402A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400880 | |||||||
| chr4:185400895 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1324-417G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400895 | |||||||
| chr4:185401202 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1324-724C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401202 | |||||||
| chr4:185401259 | A | G | 1 | a0001c0001t0005g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324-781T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401259 | |||||||
| chr4:185401349 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324-871A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401349 | |||||||
| chr4:185401442 | C | A | 1 | a0001c0001t0004g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1324-964G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401442 | |||||||
| chr4:185401458 | G | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-980C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401458 | |||||||
| chr4:185401462 | C | T | 1 | a0001c0001t0005g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1324-984G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401462 | |||||||
| chr4:185401483 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1324-1005A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401483 | |||||||
| chr4:185401587 | A | C | 1 | a0001c0001t0002g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1324-1109T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401587 | |||||||
| chr4:185401633 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1324-1155A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401633 | |||||||
| chr4:185401833 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(140): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1324-1355G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401833 | |||||||
| chr4:185402017 | C | T | 3 | a0001c0001t0002g0049 a0001c0004t0002g0015 a0002c0003t0002g0075 |
5 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+1477G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402017 | |||||||
| chr4:185402055 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(79): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1323+1439T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402055 | |||||||
| chr4:185402096 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1323+1398G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402096 | |||||||
| chr4:185402140 | CCTT | C | 25 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(22): Show |
43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.1323+1351_1323+135 others(7): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402140 | |||||||
| chr4:185402153 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1323+1341T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402153 | |||||||
| chr4:185402154 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1323+1340G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402154 | |||||||
| chr4:185402287 | A | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0080 |
3 | HG03239.hp1 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1323+1207T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402287 | |||||||
| chr4:185402294 | A | G | 19 | a0001c0001t0005g0009 a0001c0001t0005g0019 a0001c0001t0005g0027 others(16): Show |
28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1323+1200T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402294 | |||||||
| chr4:185402361 | G | GA | 6 | a0001c0001t0001g0168 a0001c0001t0001g0188 a0001c0001t0002g0066 others(3): Show |
6 | HG00741.hp1 HG02615.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+1132dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402361 | |||||||
| chr4:185402439 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1323+1055G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402439 | |||||||
| chr4:185402507 | C | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323+987G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402507 | |||||||
| chr4:185402627 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(79): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1323+867G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402627 | |||||||
| chr4:185402896 | T | C | 1 | a0001c0001t0018g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1323+598A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402896 | |||||||
| chr4:185402986 | C | T | 1 | a0001c0002t0006g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1323+508G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402986 | |||||||
| chr4:185403034 | C | T | 1 | a0001c0001t0013g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1323+460G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403034 | |||||||
| chr4:185403146 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1323+348A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403146 | |||||||
| chr4:185403255 | C | T | 20 | a0001c0001t0004g0020 a0001c0001t0004g0031 a0001c0001t0004g0111 others(17): Show |
24 | HG00408.hp2 HG00544.hp1 HG02523.hp1 others(21): Show |
intron_variant | MODIFIER | c.1323+239G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403255 | |||||||
| chr4:185403398 | C | T | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1323+96G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403398 | |||||||
| chr4:185403483 | T | C | 27 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1323+11A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403483 | |||||||
| chr4:185403687 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1199-69A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403687 | |||||||
| chr4:185403966 | C | CA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(54): Show |
96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1199-349dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | |||||||
| chr4:185403966 | C | CAA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0141 others(16): Show |
23 | HG00642.hp1 HG01433.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1199-350_1199-349d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | |||||||
| chr4:185403966 | C | CAAA | 14 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0004g0020 others(11): Show |
18 | HG00544.hp1 HG01884.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-351_1199-349d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | |||||||
| chr4:185403966 | C | CAAAA | 10 | a0001c0001t0004g0109 a0001c0001t0004g0112 a0001c0001t0004g0115 others(7): Show |
10 | HG00408.hp2 HG02738.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1199-352_1199-349d others(6): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | |||||||
| chr4:185403976 | AAC | A | 25 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(22): Show |
40 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1199-360_1199-359d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403976 | |||||||
| chr4:185403977 | AC | A | 4 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0008 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199-360delG | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403977 | |||||||
| chr4:185403978 | C | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(110): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1199-360G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403978 | |||||||
| chr4:185403988 | C | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1199-370G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403988 | |||||||
| chr4:185404042 | A | G | 1 | a0001c0001t0013g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1199-424T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404042 | |||||||
| chr4:185404075 | G | T | 1 | a0001c0001t0005g0019 | 3 | HG01975.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1199-457C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404075 | |||||||
| chr4:185404275 | T | C | 35 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(32): Show |
53 | HG00544.hp2 HG00639.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1199-657A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404275 | |||||||
| chr4:185404293 | G | GT | 39 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(36): Show |
57 | HG00544.hp2 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1199-676dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | |||||||
| chr4:185404293 | G | GTT | 7 | a0001c0001t0002g0042 a0001c0001t0002g0047 a0001c0001t0005g0094 others(4): Show |
7 | HG01433.hp2 HG02572.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199-677_1199-676d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | |||||||
| chr4:185404293 | GT | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(95): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1199-676delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | |||||||
| chr4:185404413 | A | G | 4 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0117 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-795T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404413 | |||||||
| chr4:185404560 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1199-942C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404560 | |||||||
| chr4:185404615 | T | C | 2 | a0001c0001t0002g0049 a0001c0004t0002g0015 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-997A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404615 | |||||||
| chr4:185404658 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA19054.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1199-1040G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404658 | |||||||
| chr4:185404689 | G | C | 2 | a0001c0001t0002g0049 a0001c0004t0002g0015 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-1071C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404689 | |||||||
| chr4:185405002 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(104): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1198+777dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405002 | |||||||
| chr4:185405059 | A | G | 1 | a0006c0014t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198+721T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405059 | |||||||
| chr4:185405163 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1198+617T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405163 | |||||||
| chr4:185405173 | T | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0152 |
3 | HG00408.hp1 HG02135.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1198+607A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405173 | |||||||
| chr4:185405173 | T | TG | 2 | a0001c0001t0003g0007 a0001c0001t0003g0051 |
5 | HG02074.hp1 HG02083.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198+606_1198+607i others(3): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405173 | |||||||
| chr4:185405225 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1198+555A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405225 | |||||||
| chr4:185405487 | C | A | 1 | a0001c0001t0004g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1198+293G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405487 | |||||||
| chr4:185405511 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1198+269G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405511 | |||||||
| chr4:185405555 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1198+225C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405555 | |||||||
| chr4:185405570 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1198+210G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405570 | |||||||
| chr4:185405617 | A | G | 27 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198+163T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405617 | |||||||
| chr4:185405705 | A | G | 1 | a0001c0001t0003g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1198+75T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405705 | |||||||
| chr4:185405743 | A | T | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1198+37T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405743 | |||||||
| chr4:185405868 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1122-12G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405868 | |||||||
| chr4:185405898 | A | G | 1 | a0001c0002t0006g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1122-42T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405898 | |||||||
| chr4:185405952 | G | A | 2 | a0001c0001t0008g0099 a0001c0001t0008g0101 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1122-96C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405952 | |||||||
| chr4:185406079 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(140): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1122-223G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406079 | |||||||
| chr4:185406285 | C | G | 1 | a0001c0001t0003g0017 | 3 | HG02040.hp2 HG02132.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1122-429G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406285 | |||||||
| chr4:185406359 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1122-503T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406359 | |||||||
| chr4:185406389 | G | T | 2 | a0001c0001t0002g0049 a0001c0004t0002g0015 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-533C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406389 | |||||||
| chr4:185406606 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0057 a0001c0001t0003g0059 |
4 | HG02723.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-750G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406606 | |||||||
| chr4:185406636 | C | T | 3 | a0001c0001t0003g0016 a0001c0001t0003g0050 a0001c0001t0003g0056 |
5 | NA18942.hp1 NA18945.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-780G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406636 | |||||||
| chr4:185407017 | CT | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(123): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1121+918delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | |||||||
| chr4:185407017 | CTT | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(9): Show |
14 | HG01070.hp2 HG01256.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+917_1121+918d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | |||||||
| chr4:185407017 | CTTT | C | 24 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(21): Show |
42 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1121+916_1121+918d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | |||||||
| chr4:185407017 | CTTTT | C | 19 | a0001c0001t0005g0009 a0001c0001t0005g0019 a0001c0001t0005g0027 others(16): Show |
28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1121+915_1121+918d others(6): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | |||||||
| chr4:185407048 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1121+888T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407048 | |||||||
| chr4:185407056 | G | GT | 42 | a0001c0001t0001g0146 a0001c0001t0002g0004 a0001c0001t0002g0014 others(39): Show |
69 | HG00544.hp2 HG00733.hp1 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.1121+879dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407056 | |||||||
| chr4:185407057 | T | G | 1 | a0001c0001t0005g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1121+879A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407057 | |||||||
| chr4:185407082 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1121+854C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407082 | |||||||
| chr4:185407125 | A | G | 27 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1121+811T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407125 | |||||||
| chr4:185407137 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(140): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1121+799T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407137 | |||||||
| chr4:185407318 | T | C | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1121+618A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407318 | |||||||
| chr4:185407333 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1121+603G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407333 | |||||||
| chr4:185407345 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1121+591G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407345 | |||||||
| chr4:185407439 | T | A | 8 | a0001c0001t0006g0086 a0001c0002t0006g0088 a0001c0002t0006g0089 others(5): Show |
8 | HG00639.hp1 HG01106.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+497A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407439 | |||||||
| chr4:185407550 | C | G | 1 | a0001c0006t0005g0030 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1121+386G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407550 | |||||||
| chr4:185407601 | TAA | T | 27 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1121+333_1121+334d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407601 | |||||||
| chr4:185407756 | C | T | 1 | a0006c0014t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+180G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407756 | |||||||
| chr4:185407853 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+83C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407853 | |||||||
| chr4:185408066 | T | C | 19 | a0001c0001t0005g0009 a0001c0001t0005g0019 a0001c0001t0005g0027 others(16): Show |
28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.997-6A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/11 | chr4 | 185408066 | |||||||
| chr4:185408258 | G | A | 2 | a0001c0001t0002g0066 a0001c0008t0002g0067 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.996+13C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/11 | chr4 | 185408258 | |||||||
| chr4:185408730 | A | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0051 a0001c0001t0003g0054 others(1): Show |
7 | HG00544.hp2 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-295T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408730 | |||||||
| chr4:185408807 | C | T | 1 | a0001c0002t0006g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.832-372G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408807 | |||||||
| chr4:185408927 | G | A | 26 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(23): Show |
44 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.832-492C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408927 | |||||||
| chr4:185408946 | T | C | 1 | a0001c0001t0005g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.832-511A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408946 | |||||||
| chr4:185409006 | C | T | 2 | a0001c0001t0003g0052 a0001c0001t0003g0053 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.832-571G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409006 | |||||||
| chr4:185409018 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.832-583A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409018 | |||||||
| chr4:185409043 | G | C | 1 | a0001c0002t0006g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.832-608C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409043 | |||||||
| chr4:185409258 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.832-823T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409258 | |||||||
| chr4:185409261 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.832-826C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409261 | |||||||
| chr4:185409285 | T | G | 2 | a0001c0001t0002g0049 a0001c0004t0002g0015 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-850A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409285 | |||||||
| chr4:185409324 | T | C | 28 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(25): Show |
46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.832-889A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409324 | |||||||
| chr4:185409980 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.832-1545A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409980 | |||||||
| chr4:185410021 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.832-1586A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410021 | |||||||
| chr4:185410041 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.832-1606A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410041 | |||||||
| chr4:185410045 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-1610T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410045 | |||||||
| chr4:185410332 | G | A | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-1897C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410332 | |||||||
| chr4:185410669 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01070.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.832-2234C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410669 | |||||||
| chr4:185410849 | G | GGGA | 2 | a0001c0005t0006g0026 a0001c0005t0006g0085 |
3 | HG02486.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.832-2417_832-2415d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410849 | |||||||
| chr4:185410945 | C | CA | 33 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0173 others(30): Show |
38 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.832-2511dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410945 | |||||||
| chr4:185410945 | C | CAA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(74): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.832-2512_832-2511d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410945 | |||||||
| chr4:185411119 | GT | G | 21 | a0001c0001t0002g0106 a0001c0001t0004g0020 a0001c0001t0004g0031 others(18): Show |
25 | HG00408.hp2 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.831+2606delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411119 | |||||||
| chr4:185411132 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(172): Show |
261 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.831+2594A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411132 | |||||||
| chr4:185411259 | AT | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0096 |
3 | HG02922.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.831+2466delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411259 | |||||||
| chr4:185411315 | G | A | 13 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(10): Show |
21 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+2411C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411315 | |||||||
| chr4:185411453 | G | A | 24 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(21): Show |
42 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.831+2273C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411453 | |||||||
| chr4:185411576 | A | C | 13 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(10): Show |
21 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+2150T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411576 | |||||||
| chr4:185411590 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0036 others(7): Show |
17 | HG00597.hp1 HG00738.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+2136T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411590 | |||||||
| chr4:185411622 | A | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+2104T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411622 | |||||||
| chr4:185412000 | A | G | 1 | a0001c0002t0006g0089 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.831+1726T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412000 | |||||||
| chr4:185412026 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.831+1700C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412026 | |||||||
| chr4:185412067 | A | G | 4 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0117 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+1659T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412067 | |||||||
| chr4:185412232 | T | C | 1 | a0001c0001t0006g0086 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.831+1494A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412232 | |||||||
| chr4:185412318 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.831+1408T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412318 | |||||||
| chr4:185412329 | T | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(79): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.831+1397A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412329 | |||||||
| chr4:185412753 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18986.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.831+973C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412753 | |||||||
| chr4:185412820 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.831+906C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412820 | |||||||
| chr4:185412915 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.831+811G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412915 | |||||||
| chr4:185412984 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(190): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.831+742C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412984 | |||||||
| chr4:185412985 | G | C | 1 | a0001c0001t0005g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831+741C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412985 | |||||||
| chr4:185413015 | T | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+711A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413015 | |||||||
| chr4:185413037 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.831+689C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413037 | |||||||
| chr4:185413130 | T | C | 19 | a0001c0001t0005g0009 a0001c0001t0005g0019 a0001c0001t0005g0027 others(16): Show |
28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+596A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413130 | |||||||
| chr4:185413235 | A | T | 1 | a0001c0001t0003g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.831+491T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413235 | |||||||
| chr4:185413237 | A | C | 1 | a0001c0001t0003g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.831+489T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413237 | |||||||
| chr4:185413240 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.831+486A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413240 | |||||||
| chr4:185413486 | A | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+240T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413486 | |||||||
| chr4:185413571 | T | C | 26 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(23): Show |
44 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.831+155A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413571 | |||||||
| chr4:185413645 | A | G | 28 | a0001c0001t0002g0066 a0001c0001t0003g0002 a0001c0001t0003g0007 others(25): Show |
46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.831+81T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413645 | |||||||
| chr4:185414092 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.685-220C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414092 | |||||||
| chr4:185414428 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.685-556A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414428 | |||||||
| chr4:185414456 | A | G | 1 | a0001c0001t0005g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685-584T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414456 | |||||||
| chr4:185414538 | G | A | 1 | a0001c0002t0006g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.684+617C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414538 | |||||||
| chr4:185414552 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.684+603C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414552 | |||||||
| chr4:185414588 | C | T | 10 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0042 others(7): Show |
16 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.684+567G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414588 | |||||||
| chr4:185414718 | T | A | 1 | a0001c0001t0005g0029 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.684+437A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414718 | |||||||
| chr4:185414779 | C | T | 1 | a0001c0001t0002g0004 | 5 | HG00733.hp1 HG01074.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+376G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414779 | |||||||
| chr4:185414923 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+232G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414923 | |||||||
| chr4:185415395 | CAATAAAG others(42): Show |
C | 2 | a0001c0001t0002g0066 a0001c0008t0002g0067 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.492-97_492-49delAA others(47): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415395 | |||||||
| chr4:185415418 | A | T | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.492-71T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415418 | |||||||
| chr4:185415429 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(171): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.492-82C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415429 | |||||||
| chr4:185415467 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.492-120C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415467 | |||||||
| chr4:185415514 | T | C | 13 | a0001c0002t0004g0033 a0001c0002t0004g0126 a0001c0002t0004g0127 others(10): Show |
15 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.492-167A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415514 | |||||||
| chr4:185415679 | A | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.491+31T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415679 | |||||||
| chr4:185415873 | T | C | 1 | a0001c0001t0013g0107 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.334-6A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415873 | |||||||
| chr4:185415922 | A | G | 1 | a0001c0001t0007g0116 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.334-55T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415922 | |||||||
| chr4:185415990 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-123G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415990 | |||||||
| chr4:185416045 | G | A | 2 | a0001c0001t0008g0099 a0001c0001t0008g0101 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.334-178C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416045 | |||||||
| chr4:185416383 | C | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-516G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416383 | |||||||
| chr4:185416600 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0137 a0001c0001t0001g0146 |
4 | HG02015.hp1 HG02602.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-733G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416600 | |||||||
| chr4:185416600 | CGT | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-735_334-734del others(2): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416600 | |||||||
| chr4:185416643 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-776C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416643 | |||||||
| chr4:185416833 | A | G | 1 | a0001c0001t0003g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.334-966T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416833 | |||||||
| chr4:185417052 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.334-1185G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417052 | |||||||
| chr4:185417090 | TAAGTG | T | 14 | a0001c0001t0004g0020 a0001c0001t0004g0031 a0001c0001t0004g0111 others(11): Show |
17 | HG02698.hp2 HG02738.hp1 HG04199.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-1228_334-1224d others(7): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417090 | |||||||
| chr4:185417604 | C | T | 31 | a0001c0001t0004g0020 a0001c0001t0004g0031 a0001c0001t0004g0108 others(28): Show |
35 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.333+837G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417604 | |||||||
| chr4:185417677 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0195 |
6 | HG02132.hp2 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+764A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417677 | |||||||
| chr4:185417769 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.333+672G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417769 | |||||||
| chr4:185417836 | G | A | 27 | a0001c0001t0002g0049 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
47 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+605C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417836 | |||||||
| chr4:185417920 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+521A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417920 | |||||||
| chr4:185417944 | C | T | 2 | a0001c0001t0008g0099 a0001c0001t0008g0101 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.333+497G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417944 | |||||||
| chr4:185417961 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.333+480A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417961 | |||||||
| chr4:185418047 | A | AACAC | 3 | a0001c0001t0016g0110 a0001c0005t0006g0026 a0001c0005t0006g0085 |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+390_333+393dup others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(5): Show |
3 | a0001c0001t0001g0189 a0001c0001t0003g0065 a0002c0003t0002g0079 |
3 | HG02970.hp1 HG02970.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.333+382_333+393dup others(12): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(7): Show |
26 | a0001c0001t0001g0038 a0001c0001t0001g0185 a0001c0001t0001g0186 others(23): Show |
30 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.333+380_333+393dup others(14): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(9): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0134 a0001c0001t0001g0180 others(9): Show |
16 | HG00733.hp2 HG01106.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+378_333+393dup others(16): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(11): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(79): Show |
137 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.333+376_333+393dup others(18): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(13): Show |
22 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0139 others(19): Show |
31 | HG01074.hp2 HG01255.hp1 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.333+374_333+393dup others(20): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(15): Show |
9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0002g0024 others(6): Show |
11 | HG00140.hp2 HG01515.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(22): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(17): Show |
6 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0066 others(3): Show |
13 | HG01192.hp2 HG01243.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(24): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(19): Show |
6 | a0001c0001t0002g0005 a0001c0001t0005g0097 a0001c0001t0005g0098 others(3): Show |
10 | HG00642.hp2 HG00741.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(26): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(21): Show |
3 | a0001c0001t0005g0009 a0001c0001t0005g0019 a0001c0001t0005g0029 |
9 | HG01975.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(28): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(23): Show |
5 | a0001c0001t0005g0027 a0001c0001t0005g0092 a0001c0001t0005g0094 others(2): Show |
6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(30): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | AACACACA others(27): Show |
2 | a0001c0001t0005g0028 a0001c0001t0005g0093 |
3 | HG02809.hp2 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.333+393_333+394ins others(34): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(17): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(19): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418047 | A | ACACACAC others(14): Show |
1 | a0001c0001t0002g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(21): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | |||||||
| chr4:185418068 | A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.333+372_333+373ins others(17): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418068 | |||||||
| chr4:185418068 | A | ACACACAC others(16): Show |
1 | a0001c0001t0003g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.333+372_333+373ins others(23): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418068 | |||||||
| chr4:185418069 | A | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0042 others(7): Show |
12 | HG01081.hp2 HG01255.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+372T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418069 | |||||||
| chr4:185418069 | A | T | 1 | a0001c0001t0002g0004 | 5 | HG00733.hp1 HG01074.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+372T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418069 | |||||||
| chr4:185418071 | C | CACACACA others(4): Show |
10 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(7): Show |
16 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+369_333+370ins others(11): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418071 | |||||||
| chr4:185418080 | C | T | 27 | a0001c0001t0002g0049 a0001c0001t0003g0002 a0001c0001t0003g0007 others(24): Show |
47 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+361G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418080 | |||||||
| chr4:185418143 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.333+298A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418143 | |||||||
| chr4:185418164 | T | C | 2 | a0001c0001t0008g0099 a0001c0001t0008g0101 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.333+277A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418164 | |||||||
| chr4:185418295 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(111): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.333+146T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418295 | |||||||
| chr4:185418430 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(192): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.333+11T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418430 | |||||||
| chr4:185419154 | T | C | 11 | a0001c0002t0004g0033 a0001c0002t0004g0126 a0001c0002t0004g0127 others(8): Show |
13 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-384A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419154 | |||||||
| chr4:185419195 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.83-425C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419195 | |||||||
| chr4:185419200 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.83-430C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419200 | |||||||
| chr4:185419225 | G | A | 1 | a0001c0001t0011g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.83-455C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419225 | |||||||
| chr4:185419256 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.83-486G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419256 | |||||||
| chr4:185419377 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83-607C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419377 | |||||||
| chr4:185419382 | G | A | 1 | a0001c0001t0008g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.83-612C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419382 | |||||||
| chr4:185419410 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(192): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.83-640T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419410 | |||||||
| chr4:185419709 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.83-939A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419709 | |||||||
| chr4:185419723 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.83-953A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419723 | |||||||
| chr4:185419818 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG00140.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.83-1048A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419818 | |||||||
| chr4:185420006 | G | A | 12 | a0001c0002t0004g0033 a0001c0002t0004g0126 a0001c0002t0004g0127 others(9): Show |
13 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-1236C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420006 | |||||||
| chr4:185420080 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.83-1310A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420080 | |||||||
| chr4:185420183 | GT | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(192): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.83-1414delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420183 | |||||||
| chr4:185420299 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83-1529A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420299 | |||||||
| chr4:185420655 | C | T | 1 | a0001c0002t0006g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82+1830G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420655 | |||||||
| chr4:185420771 | T | C | 1 | a0001c0002t0006g0091 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82+1714A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420771 | |||||||
| chr4:185420846 | T | C | 26 | a0001c0001t0002g0049 a0001c0001t0003g0002 a0001c0001t0003g0007 others(23): Show |
46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.82+1639A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420846 | |||||||
| chr4:185420847 | T | C | 1 | a0001c0001t0004g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+1638A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420847 | |||||||
| chr4:185420928 | T | G | 1 | a0001c0001t0005g0029 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.82+1557A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420928 | |||||||
| chr4:185420976 | T | C | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82+1509A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420976 | |||||||
| chr4:185421122 | GCTGA | G | 3 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0016g0110 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.82+1359_82+1362del others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421122 | |||||||
| chr4:185421373 | T | C | 28 | a0001c0001t0002g0049 a0001c0001t0002g0066 a0001c0001t0003g0002 others(25): Show |
48 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.82+1112A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421373 | |||||||
| chr4:185421388 | G | A | 1 | a0001c0008t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82+1097C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421388 | |||||||
| chr4:185421693 | C | T | 1 | a0001c0001t0005g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+792G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421693 | |||||||
| chr4:185421701 | C | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(114): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.82+784G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421701 | |||||||
| chr4:185422228 | T | C | 2 | a0001c0001t0010g0193 a0001c0001t0010g0197 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.82+257A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185422228 | |||||||
| chr4:185422706 | T | C | 13 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(10): Show |
20 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.4-143A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422706 | |||||||
| chr4:185422761 | T | G | 15 | a0001c0001t0004g0020 a0001c0001t0004g0120 a0001c0001t0004g0121 others(12): Show |
19 | HG00408.hp2 HG00544.hp1 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.4-198A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422761 | |||||||
| chr4:185422811 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4-248G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422811 | |||||||
| chr4:185422825 | A | G | 13 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(10): Show |
20 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.4-262T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422825 | |||||||
| chr4:185422903 | A | AG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(190): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.4-341dupC | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422903 | |||||||
| chr4:185422936 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4-373C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422936 | |||||||
| chr4:185422976 | A | G | 1 | a0001c0001t0005g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4-413T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422976 | |||||||
| chr4:185423034 | T | G | 2 | a0001c0001t0002g0066 a0001c0008t0002g0067 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4-471A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423034 | |||||||
| chr4:185423139 | G | A | 41 | a0001c0001t0002g0049 a0001c0001t0003g0002 a0001c0001t0003g0007 others(38): Show |
65 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.4-576C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423139 | |||||||
| chr4:185423148 | C | T | 20 | a0001c0001t0002g0106 a0001c0001t0005g0009 a0001c0001t0005g0019 others(17): Show |
29 | HG00642.hp2 HG00733.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-585G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423148 | |||||||
| chr4:185423361 | T | C | 1 | a0003c0007t0005g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4-798A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423361 | |||||||
| chr4:185423379 | G | A | 1 | a0001c0006t0005g0030 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4-816C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423379 | |||||||
| chr4:185423563 | TA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(84): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.4-1001delT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423563 | |||||||
| chr4:185423648 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4-1085A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423648 | |||||||
| chr4:185423813 | TAC | T | 3 | a0001c0001t0001g0134 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01258.hp2 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4-1252_4-1251delGT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423813 | |||||||
| chr4:185424031 | T | C | 3 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0016g0110 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4-1468A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424031 | |||||||
| chr4:185424100 | G | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0062 a0001c0001t0003g0063 others(2): Show |
8 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-1537C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424100 | |||||||
| chr4:185424140 | CA | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(127): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-1578delT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424140 | |||||||
| chr4:185424229 | C | T | 3 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0016g0110 |
3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3+1637G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424229 | |||||||
| chr4:185424230 | G | A | 23 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(20): Show |
41 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3+1636C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424230 | |||||||
| chr4:185424252 | G | A | 1 | a0001c0002t0006g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3+1614C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424252 | |||||||
| chr4:185424374 | A | G | 11 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0041 others(8): Show |
17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+1492T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424374 | |||||||
| chr4:185424577 | G | A | 26 | a0001c0001t0002g0049 a0001c0001t0003g0002 a0001c0001t0003g0007 others(23): Show |
46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.3+1289C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424577 | |||||||
| chr4:185424626 | C | A | 2 | a0001c0001t0002g0066 a0001c0008t0002g0067 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3+1240G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424626 | |||||||
| chr4:185424689 | T | A | 1 | a0001c0002t0006g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3+1177A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424689 | |||||||
| chr4:185424716 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+1150C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424716 | |||||||
| chr4:185424879 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3+987A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424879 | |||||||
| chr4:185424998 | C | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(173): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.3+868G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424998 | |||||||
| chr4:185425085 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(145): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.3+781G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425085 | |||||||
| chr4:185425315 | T | C | 2 | a0001c0002t0004g0129 a0001c0002t0004g0130 |
2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3+551A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425315 | |||||||
| chr4:185425372 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3+494C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425372 | |||||||
| chr4:185425553 | G | C | 1 | a0001c0001t0010g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3+313C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425553 | |||||||
| chr4:185425570 | C | A | 1 | a0001c0001t0019g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3+296G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425570 | |||||||
| chr4:185425716 | A | G | 13 | a0001c0001t0001g0132 a0001c0001t0002g0004 a0001c0001t0002g0014 others(10): Show |
19 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.3+150T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425716 | |||||||
| chr4:185425749 | G | A | 1 | a0001c0001t0004g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3+117C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425749 | |||||||
| chr4:185425834 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3+32G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425834 |