Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23376 |
| ensemblid | ENSG00000014123.10 |
| hgncid | 23039 |
| symbol | UFL1 |
| name | UFM1 specific ligase 1 |
| refseq_nuc | NM_015323.5 |
| refseq_prot | NP_056138.1 |
| ensembl_nuc | ENST00000369278.5 |
| ensembl_prot | ENSP00000358283.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 96521806 |
| end | 96555276 |
| strand | + |
| ver | v1.2 |
| region | chr6:96521806-96555276 |
| region5000 | chr6:96516806-96560276 |
| regionname0 | UFL1_chr6_96521806_96555276 |
| regionname5000 | UFL1_chr6_96516806_96560276 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 794 | 360 | 80 | 64 | 161 | 14 | 39 | 130 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0002 | 0/0 | 794 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0003 | 0/0 | 794 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0004 | 0/0 | 794 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0005 | 0/0 | 794 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0006 | 0/0 | 794 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0007 | 0/0 | 794 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| a0008 | 0/0 | 794 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | MADAW others(789): Show |
chr6 | 96516806 | 96560276 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2382 | 196 | 51 | 40 | 77 | 5 | 22 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0002 | 0/1 | 2382 | 143 | 25 | 19 | 76 | 6 | 16 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0003 | 0/0 | 2382 | 8 | 2 | 4 | 0 | 2 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0004 | 0/0 | 2382 | 7 | 0 | 0 | 7 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0011 | 0/0 | 2382 | 2 | 1 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0012 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0014 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0015 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0001c0016 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0002c0005 | 0/0 | 2382 | 6 | 0 | 0 | 6 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0003c0006 | 0/0 | 2382 | 5 | 0 | 0 | 5 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0004c0007 | 0/0 | 2382 | 4 | 0 | 0 | 4 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0005c0009 | 0/0 | 2382 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0006c0008 | 0/0 | 2382 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0007c0010 | 0/0 | 2382 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 | ||
| a0008c0013 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | ATGGC others(2377): Show |
chr6 | 96516806 | 96560276 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4226 | 187 | 46 | 38 | 77 | 5 | 20 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0001t0006 | 0/0 | 4226 | 4 | 3 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0001t0010 | 0/0 | 4226 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0001t0014 | 0/0 | 4226 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0001t0018 | 0/0 | 4226 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0001t0023 | 0/0 | 4226 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0001 | 0/1 | 4226 | 80 | 12 | 6 | 53 | 0 | 8 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0002 | 0/0 | 4226 | 47 | 4 | 11 | 20 | 5 | 7 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0005 | 0/0 | 4226 | 5 | 5 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0008 | 0/0 | 4226 | 2 | 0 | 1 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0009 | 0/0 | 4226 | 2 | 0 | 1 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0011 | 0/0 | 4226 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0013 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0015 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0016 | 0/0 | 4226 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0017 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0002t0020 | 0/0 | 4226 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0003t0001 | 0/0 | 4226 | 2 | 1 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0003t0004 | 0/0 | 4226 | 6 | 1 | 3 | 0 | 2 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0004t0003 | 0/0 | 4226 | 6 | 0 | 0 | 6 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0004t0019 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0011t0012 | 0/0 | 4226 | 2 | 1 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0012t0001 | 0/0 | 4226 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0014t0001 | 0/0 | 4226 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0015t0001 | 0/0 | 4226 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0001c0016t0001 | 0/0 | 4226 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0002c0005t0001 | 0/0 | 4226 | 6 | 0 | 0 | 6 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0003c0006t0001 | 0/0 | 4226 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0003c0006t0007 | 0/0 | 4226 | 3 | 0 | 0 | 3 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0004c0007t0001 | 0/0 | 4226 | 4 | 0 | 0 | 4 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0005c0009t0001 | 0/0 | 4226 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0006c0008t0001 | 0/0 | 4226 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0007c0010t0021 | 0/0 | 4226 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0007c0010t0022 | 0/0 | 4226 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| a0008c0013t0001 | 0/0 | 4226 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | CTCTT others(4221): Show |
chr6 | 96516806 | 96560276 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 47 | 3 | 16 | 23 | 1 | 4 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0004 | 0/0 | 17 | 1 | 6 | 8 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0007 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0008 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0010 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0010g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0018g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0001t0023g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0003 | 0/0 | 19 | 0 | 0 | 19 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0005 | 0/0 | 10 | 1 | 1 | 6 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0006 | 0/0 | 12 | 0 | 0 | 9 | 0 | 3 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0002 | 0/0 | 26 | 0 | 6 | 16 | 1 | 3 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0005g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0008g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0009g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0011g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0002t0020g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0003t0004g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0003t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0004t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0004t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0011t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0011t0012g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0014t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0015t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0001c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0002c0005t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0002c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0003c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0003c0006t0007g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0003c0006t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0004c0007t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0004c0007t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0005c0009t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0006c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0006c0008t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0007c0010t0021g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0007c0010t0022g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| a0008c0013t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0151 | EUR | FIN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00323 | hp1 | a0001 | c0002 | t0009 | g0142 | EUR | FIN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0086 | EUR | FIN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00408 | hp1 | a0001 | c0014 | t0001 | g0008 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00438 | hp1 | a0004 | c0007 | t0001 | g0001 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00438 | hp2 | a0003 | c0006 | t0001 | g0001 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00558 | hp2 | a0004 | c0007 | t0001 | g0114 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00621 | hp1 | a0001 | c0004 | t0003 | g0015 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00621 | hp2 | a0002 | c0005 | t0001 | g0005 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01070 | hp1 | a0001 | c0003 | t0004 | g0084 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0018 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01081 | hp1 | a0001 | c0001 | t0018 | g0026 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0018 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0145 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0065 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0073 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0034 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01515 | hp2 | a0001 | c0012 | t0001 | g0001 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01516 | hp2 | a0001 | c0003 | t0004 | g0032 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01517 | hp1 | a0001 | c0003 | t0004 | g0032 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0034 | EUR | IBS | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01891 | hp1 | a0001 | c0011 | t0012 | g0136 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02015 | hp1 | a0001 | c0002 | t0015 | g0003 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0018 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CDX | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02165 | hp1 | a0002 | c0005 | t0001 | g0143 | EAS | CDX | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02293 | hp1 | a0001 | c0011 | t0012 | g0137 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02300 | hp2 | a0001 | c0002 | t0008 | g0033 | AMR | PEL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02451 | hp2 | a0005 | c0009 | t0001 | g0022 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02602 | hp1 | a0001 | c0002 | t0008 | g0033 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02602 | hp2 | a0008 | c0013 | t0001 | g0004 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02738 | hp1 | a0001 | c0016 | t0001 | g0050 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02965 | hp1 | a0006 | c0008 | t0001 | g0060 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02965 | hp2 | a0007 | c0010 | t0022 | g0093 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02970 | hp2 | a0001 | c0002 | t0016 | g0135 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03041 | hp1 | a0001 | c0002 | t0011 | g0036 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03130 | hp2 | a0001 | c0002 | t0005 | g0078 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03453 | hp1 | a0007 | c0010 | t0021 | g0094 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03540 | hp2 | a0001 | c0015 | t0001 | g0054 | AFR | GWD | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03579 | hp1 | a0001 | c0002 | t0011 | g0036 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03669 | hp1 | a0001 | c0001 | t0023 | g0139 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03669 | hp2 | a0001 | c0001 | t0014 | g0106 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0031 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0031 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18950 | hp2 | a0001 | c0002 | t0013 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18951 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18963 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18975 | hp1 | a0004 | c0007 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18980 | hp2 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18984 | hp2 | a0001 | c0002 | t0017 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18994 | hp2 | a0001 | c0004 | t0019 | g0039 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18997 | hp1 | a0001 | c0004 | t0003 | g0015 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19001 | hp2 | a0003 | c0006 | t0007 | g0044 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19007 | hp2 | a0001 | c0004 | t0003 | g0015 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0097 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19011 | hp1 | a0003 | c0006 | t0007 | g0044 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19054 | hp1 | a0001 | c0004 | t0003 | g0039 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19066 | hp2 | a0003 | c0006 | t0007 | g0102 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19076 | hp1 | a0004 | c0007 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19081 | hp1 | a0001 | c0004 | t0003 | g0015 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19086 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19091 | hp1 | a0003 | c0006 | t0001 | g0001 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA19240 | hp2 | a0006 | c0008 | t0001 | g0055 | AFR | YRI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ASW | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ASW | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA20300 | hp2 | a0005 | c0009 | t0001 | g0022 | AFR | USA | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA21309 | hp1 | a0001 | c0002 | t0020 | g0082 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | LWK | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0147 | REF | REF | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0061 | REF | REF | UFL1_chr6_96516806_96560276 | UFL1 | chr6 | 96516806 | 96560276 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96525298 | T | G | 1 | a0006 | 2 | HG02965.hp1 NA19240.hp2 |
missense_variant&splice_region_variant | MODERATE | c.254T>G | p.Val85Gly | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 4/19 | 322/4226 | 254/2385 | 85/794 | chr6 | 96525298 | |||
| chr6:96526379 | G | T | 1 | a0002 | 6 | HG00621.hp2 HG02165.hp1 NA18951.hp1 others(3): Show |
missense_variant | MODERATE | c.409G>T | p.Val137Phe | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/19 | 477/4226 | 409/2385 | 137/794 | chr6 | 96526379 | |||
| chr6:96528520 | G | A | 1 | a0005 | 2 | HG02451.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.484G>A | p.Gly162Ser | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/19 | 552/4226 | 484/2385 | 162/794 | chr6 | 96528520 | |||
| chr6:96540604 | G | A | 1 | a0004 | 4 | HG00438.hp1 HG00558.hp2 NA18975.hp1 others(1): Show |
missense_variant | MODERATE | c.1228G>A | p.Val410Ile | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/19 | 1296/4226 | 1228/2385 | 410/794 | chr6 | 96540604 | |||
| chr6:96548257 | C | T | 1 | a0003 | 5 | HG00438.hp2 NA19001.hp2 NA19011.hp1 others(2): Show |
missense_variant | MODERATE | c.1496C>T | p.Ser499Leu | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/19 | 1564/4226 | 1496/2385 | 499/794 | chr6 | 96548257 | |||
| chr6:96552489 | C | G | 1 | a0007 | 2 | HG02965.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1993C>G | p.Leu665Val | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 18/19 | 2061/4226 | 1993/2385 | 665/794 | chr6 | 96552489 | |||
| chr6:96552606 | G | A | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2110G>A | p.Ala704Thr | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 18/19 | 2178/4226 | 2110/2385 | 704/794 | chr6 | 96552606 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96523263 | A | G | 1 | a0001c0004 | 7 | HG00621.hp1 NA18994.hp2 NA18997.hp1 others(4): Show |
synonymous_variant | LOW | c.195A>G | p.Glu65Glu | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/19 | 263/4226 | 195/2385 | 65/794 | chr6 | 96523263 | |||
| chr6:96537435 | T | C | 1 | a0001c0003 | 8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
synonymous_variant | LOW | c.864T>C | p.Tyr288Tyr | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/19 | 932/4226 | 864/2385 | 288/794 | chr6 | 96537435 | |||
| chr6:96549433 | C | T | 1 | a0001c0016 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1542C>T | p.Leu514Leu | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 14/19 | 1610/4226 | 1542/2385 | 514/794 | chr6 | 96549433 | |||
| chr6:96549532 | G | A | 1 | a0001c0012 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1641G>A | p.Leu547Leu | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 14/19 | 1709/4226 | 1641/2385 | 547/794 | chr6 | 96549532 | |||
| chr6:96549541 | C | T | 1 | a0001c0015 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1650C>T | p.Asn550Asn | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 14/19 | 1718/4226 | 1650/2385 | 550/794 | chr6 | 96549541 | |||
| chr6:96549775 | C | T | 1 | a0001c0011 | 2 | HG01891.hp1 HG02293.hp1 |
synonymous_variant | LOW | c.1794C>T | p.Asp598Asp | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/19 | 1862/4226 | 1794/2385 | 598/794 | chr6 | 96549775 | |||
| chr6:96551459 | A | G | 1 | a0001c0014 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1845A>G | p.Leu615Leu | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 16/19 | 1913/4226 | 1845/2385 | 615/794 | chr6 | 96551459 | |||
| chr6:96551849 | C | T | 6 | a0001c0002 a0001c0003 a0001c0015 others(3): Show |
160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
synonymous_variant | LOW | c.1911C>T | p.Asp637Asp | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/19 | 1979/4226 | 1911/2385 | 637/794 | chr6 | 96551849 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96521818 | C | A | 4 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0008 others(1): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-56C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/19 | 56 | chr6 | 96521818 | ||||||
| chr6:96521842 | G | C | 1 | a0001c0002t0009 | 2 | HG00323.hp1 HG01106.hp2 |
5_prime_UTR_variant | MODIFIER | c.-32G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/19 | 32 | chr6 | 96521842 | ||||||
| chr6:96553592 | C | G | 1 | a0001c0001t0023 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 89 | chr6 | 96553592 | ||||||
| chr6:96553870 | G | A | 1 | a0001c0001t0014 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 367 | chr6 | 96553870 | ||||||
| chr6:96553895 | C | T | 2 | a0007c0010t0021 a0007c0010t0022 |
2 | HG02965.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 392 | chr6 | 96553895 | ||||||
| chr6:96553958 | T | A | 1 | a0003c0006t0007 | 3 | NA19001.hp2 NA19011.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*455T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 455 | chr6 | 96553958 | ||||||
| chr6:96554086 | T | A | 1 | a0001c0002t0015 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 583 | chr6 | 96554086 | ||||||
| chr6:96554133 | C | T | 1 | a0001c0002t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 630 | chr6 | 96554133 | ||||||
| chr6:96554201 | G | A | 1 | a0001c0001t0010 | 2 | NA18522.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*698G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 698 | chr6 | 96554201 | ||||||
| chr6:96554292 | G | A | 1 | a0001c0002t0016 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 789 | chr6 | 96554292 | ||||||
| chr6:96554295 | C | T | 1 | a0001c0004t0019 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 792 | chr6 | 96554295 | ||||||
| chr6:96554367 | G | A | 1 | a0001c0002t0017 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*864G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 864 | chr6 | 96554367 | ||||||
| chr6:96554457 | G | A | 2 | a0001c0004t0003 a0001c0004t0019 |
7 | HG00621.hp1 NA18994.hp2 NA18997.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 954 | chr6 | 96554457 | ||||||
| chr6:96554494 | A | G | 1 | a0007c0010t0022 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*991A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 991 | chr6 | 96554494 | ||||||
| chr6:96554622 | C | G | 1 | a0001c0002t0008 | 2 | HG02300.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1119C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1119 | chr6 | 96554622 | ||||||
| chr6:96554755 | A | T | 1 | a0001c0001t0018 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1252A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1252 | chr6 | 96554755 | ||||||
| chr6:96554785 | C | A | 1 | a0001c0003t0004 | 6 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1282C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1282 | chr6 | 96554785 | ||||||
| chr6:96554785 | C | T | 1 | a0001c0002t0013 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1282 | chr6 | 96554785 | ||||||
| chr6:96554833 | A | G | 1 | a0001c0011t0012 | 2 | HG01891.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1330 | chr6 | 96554833 | ||||||
| chr6:96554871 | T | A | 1 | a0001c0002t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1368T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1368 | chr6 | 96554871 | ||||||
| chr6:96554890 | A | G | 1 | a0001c0002t0011 | 2 | HG03041.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1387A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1387 | chr6 | 96554890 | ||||||
| chr6:96554900 | G | T | 1 | a0001c0003t0004 | 6 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1397G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1397 | chr6 | 96554900 | ||||||
| chr6:96554969 | G | T | 1 | a0007c0010t0022 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1466 | chr6 | 96554969 | ||||||
| chr6:96555158 | C | T | 1 | a0001c0002t0005 | 5 | HG02486.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1655C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1655 | chr6 | 96555158 | ||||||
| chr6:96555238 | A | G | 1 | a0001c0001t0006 | 4 | HG01109.hp1 HG03453.hp2 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1735A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 19/19 | 1735 | chr6 | 96555238 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:96522002 | C | T | 1 | a0001c0002t0002g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.77+52C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522002 | |||||||
| chr6:96522039 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.77+89A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522039 | |||||||
| chr6:96522041 | C | T | 15 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0027 others(12): Show |
52 | HG00323.hp1 HG00544.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.77+91C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522041 | |||||||
| chr6:96522209 | G | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG03654.hp2 HG03669.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+259G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522209 | |||||||
| chr6:96522224 | G | A | 1 | a0001c0002t0001g0029 | 2 | HG00673.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.77+274G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522224 | |||||||
| chr6:96522377 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0048 |
4 | HG02451.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+427G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522377 | |||||||
| chr6:96522421 | C | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.77+471C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522421 | |||||||
| chr6:96522521 | T | G | 1 | a0001c0001t0010g0031 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.77+571T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522521 | |||||||
| chr6:96522522 | T | C | 1 | a0001c0001t0010g0031 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.77+572T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522522 | |||||||
| chr6:96522615 | C | T | 1 | a0001c0002t0016g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.78-531C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | chr6 | 96522615 | |||||||
| chr6:96522978 | G | GT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(56): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.78-159dupT | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 96522978 | ||||||
| chr6:96523310 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0066 |
7 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+19T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523310 | |||||||
| chr6:96523341 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223+50A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523341 | |||||||
| chr6:96523612 | AG | A | 2 | a0001c0002t0001g0024 a0001c0002t0001g0095 |
4 | HG01168.hp1 HG01169.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+323delG | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 96523612 | ||||||
| chr6:96523628 | G | T | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.223+337G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523628 | |||||||
| chr6:96523670 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.223+379G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523670 | |||||||
| chr6:96523726 | T | C | 4 | a0001c0004t0003g0015 a0001c0004t0003g0039 a0001c0004t0003g0097 others(1): Show |
7 | HG00621.hp1 NA18994.hp2 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+435T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523726 | |||||||
| chr6:96523744 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.223+453A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523744 | |||||||
| chr6:96523776 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.223+485A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523776 | |||||||
| chr6:96523784 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(30): Show |
84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.223+493T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523784 | |||||||
| chr6:96523807 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
5 | HG00597.hp2 HG02074.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+516G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523807 | |||||||
| chr6:96523927 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(71): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.224-455C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96523927 | |||||||
| chr6:96524050 | G | A | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.224-332G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96524050 | |||||||
| chr6:96524160 | T | C | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.224-222T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96524160 | |||||||
| chr6:96524167 | TA | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0132 a0001c0002t0001g0149 others(5): Show |
9 | HG00323.hp2 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-199delA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 96524167 | ||||||
| chr6:96524289 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224-93A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96524289 | |||||||
| chr6:96524307 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.224-75A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 2/18 | chr6 | 96524307 | |||||||
| chr6:96524522 | G | A | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.252+112G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524522 | |||||||
| chr6:96524541 | C | T | 1 | a0001c0011t0012g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.252+131C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524541 | |||||||
| chr6:96524565 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.252+155C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524565 | |||||||
| chr6:96524658 | T | C | 4 | a0001c0011t0012g0136 a0001c0011t0012g0137 a0007c0010t0021g0094 others(1): Show |
4 | HG01891.hp1 HG02293.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+248T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524658 | |||||||
| chr6:96524931 | A | C | 1 | a0001c0002t0002g0085 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.253-366A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524931 | |||||||
| chr6:96524992 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.253-305C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96524992 | |||||||
| chr6:96525021 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0148 |
3 | NA18968.hp1 NA18995.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.253-276C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96525021 | |||||||
| chr6:96525033 | G | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(10): Show |
38 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.253-264G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96525033 | |||||||
| chr6:96525147 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.253-150C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96525147 | |||||||
| chr6:96525202 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
7 | HG00733.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-95G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96525202 | |||||||
| chr6:96525265 | A | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.253-32A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 3/18 | chr6 | 96525265 | |||||||
| chr6:96525487 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(30): Show |
84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.350+93G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 4/18 | chr6 | 96525487 | |||||||
| chr6:96525679 | TA | T | 9 | a0001c0001t0001g0091 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
11 | HG01070.hp1 HG01168.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.350+304delA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 96525679 | ||||||
| chr6:96526044 | C | A | 1 | a0001c0002t0009g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.351-277C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 4/18 | chr6 | 96526044 | |||||||
| chr6:96526085 | C | CA | 6 | a0001c0001t0001g0101 a0001c0003t0001g0072 a0001c0003t0001g0073 others(3): Show |
9 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.351-224dupA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 96526085 | ||||||
| chr6:96526510 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(140): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.465+75A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526510 | |||||||
| chr6:96526511 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.465+76A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526511 | |||||||
| chr6:96526514 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.465+79A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526514 | |||||||
| chr6:96526572 | T | C | 1 | a0001c0002t0008g0033 | 2 | HG02300.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.465+137T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526572 | |||||||
| chr6:96526709 | C | A | 12 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0029 others(9): Show |
26 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.465+274C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526709 | |||||||
| chr6:96526718 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.465+283A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526718 | |||||||
| chr6:96526943 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.465+508A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526943 | |||||||
| chr6:96526953 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(156): Show |
378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.465+518A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526953 | |||||||
| chr6:96526995 | A | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.465+560A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96526995 | |||||||
| chr6:96527052 | T | G | 2 | a0001c0002t0001g0057 a0001c0015t0001g0054 |
2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.465+617T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527052 | |||||||
| chr6:96527133 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.465+698T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527133 | |||||||
| chr6:96527351 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(71): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.465+916A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527351 | |||||||
| chr6:96527437 | C | CT | 12 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0029 others(9): Show |
26 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.465+1003dupT | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 96527437 | ||||||
| chr6:96527479 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.466-1023G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527479 | |||||||
| chr6:96527621 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.466-881C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527621 | |||||||
| chr6:96527628 | A | G | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.466-874A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527628 | |||||||
| chr6:96527669 | T | TA | 3 | a0001c0002t0001g0057 a0001c0002t0001g0059 a0001c0015t0001g0054 |
3 | HG02886.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.466-832dupA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 96527669 | ||||||
| chr6:96527738 | A | G | 6 | a0001c0002t0001g0012 a0001c0002t0001g0069 a0001c0002t0001g0070 others(3): Show |
10 | HG00733.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-764A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527738 | |||||||
| chr6:96527996 | T | C | 1 | a0001c0002t0001g0027 | 3 | NA18981.hp1 NA18989.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.466-506T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96527996 | |||||||
| chr6:96528005 | C | T | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.466-497C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528005 | |||||||
| chr6:96528106 | A | G | 1 | a0001c0002t0001g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-396A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528106 | |||||||
| chr6:96528144 | C | T | 1 | a0001c0002t0002g0034 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.466-358C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528144 | |||||||
| chr6:96528194 | A | G | 1 | a0001c0002t0001g0029 | 2 | HG00673.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.466-308A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528194 | |||||||
| chr6:96528328 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0023g0139 |
2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.466-174G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528328 | |||||||
| chr6:96528373 | T | G | 1 | a0003c0006t0007g0102 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.466-129T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 5/18 | chr6 | 96528373 | |||||||
| chr6:96528702 | C | T | 2 | a0001c0002t0001g0057 a0001c0015t0001g0054 |
2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.596+70C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96528702 | |||||||
| chr6:96528884 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(141): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.596+252T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96528884 | |||||||
| chr6:96528986 | T | C | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.596+354T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96528986 | |||||||
| chr6:96529070 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.596+438T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529070 | |||||||
| chr6:96529174 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.596+542G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529174 | |||||||
| chr6:96529275 | A | G | 1 | a0001c0001t0001g0023 | 3 | HG01496.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.596+643A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529275 | |||||||
| chr6:96529355 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0150 |
6 | NA18947.hp1 NA18949.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+723G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529355 | |||||||
| chr6:96529509 | TCC | T | 3 | a0001c0002t0001g0057 a0001c0002t0001g0059 a0001c0015t0001g0054 |
3 | HG02886.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.596+878_596+879del others(2): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529509 | |||||||
| chr6:96529511 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(146): Show |
365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.596+879C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529511 | |||||||
| chr6:96529754 | C | T | 2 | a0001c0002t0002g0019 a0001c0002t0002g0083 |
4 | HG02257.hp1 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+1122C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529754 | |||||||
| chr6:96529958 | T | G | 1 | a0001c0002t0002g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.596+1326T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96529958 | |||||||
| chr6:96530680 | C | A | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.596+2048C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96530680 | |||||||
| chr6:96530848 | C | T | 1 | a0001c0003t0001g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.596+2216C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96530848 | |||||||
| chr6:96531045 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.596+2413G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531045 | |||||||
| chr6:96531148 | C | T | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.596+2516C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531148 | |||||||
| chr6:96531187 | A | G | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.596+2555A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531187 | |||||||
| chr6:96531248 | CAT | C | 46 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(43): Show |
105 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.596+2617_596+2618d others(4): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531248 | |||||||
| chr6:96531249 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.596+2617A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531249 | |||||||
| chr6:96531897 | A | G | 46 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(43): Show |
105 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.597-2366A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531897 | |||||||
| chr6:96531960 | T | A | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0004g0018 others(2): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-2303T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96531960 | |||||||
| chr6:96532104 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.597-2159T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532104 | |||||||
| chr6:96532115 | C | T | 12 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0029 others(9): Show |
26 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.597-2148C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532115 | |||||||
| chr6:96532374 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.597-1889C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532374 | |||||||
| chr6:96532511 | T | C | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.597-1752T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532511 | |||||||
| chr6:96532542 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.597-1721G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532542 | |||||||
| chr6:96532683 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.597-1580A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532683 | |||||||
| chr6:96532780 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.597-1483T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532780 | |||||||
| chr6:96532975 | A | G | 1 | a0001c0002t0002g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.597-1288A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96532975 | |||||||
| chr6:96533080 | G | A | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.597-1183G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533080 | |||||||
| chr6:96533221 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.597-1042A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533221 | |||||||
| chr6:96533290 | A | T | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597-973A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533290 | |||||||
| chr6:96533300 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.597-963A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533300 | |||||||
| chr6:96533313 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(56): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.597-950G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533313 | |||||||
| chr6:96533599 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0150 |
6 | NA18947.hp1 NA18949.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.597-664A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533599 | |||||||
| chr6:96533610 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.597-653G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533610 | |||||||
| chr6:96533799 | C | CA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(63): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.597-446dupA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 96533799 | ||||||
| chr6:96533799 | C | CAA | 7 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0025 others(4): Show |
15 | HG00741.hp1 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-447_597-446dup others(2): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 96533799 | ||||||
| chr6:96533799 | CA | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0067 others(30): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.597-446delA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 96533799 | ||||||
| chr6:96533870 | A | C | 1 | a0001c0002t0002g0079 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.597-393A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533870 | |||||||
| chr6:96533950 | G | C | 1 | a0001c0002t0001g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.597-313G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96533950 | |||||||
| chr6:96534143 | G | T | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597-120G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 6/18 | chr6 | 96534143 | |||||||
| chr6:96534424 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655+103A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96534424 | |||||||
| chr6:96534624 | A | C | 1 | a0001c0004t0003g0097 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.655+303A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96534624 | |||||||
| chr6:96534684 | G | T | 1 | a0001c0002t0001g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.655+363G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96534684 | |||||||
| chr6:96534841 | T | G | 1 | a0001c0002t0001g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.655+520T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96534841 | |||||||
| chr6:96534855 | A | AT | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0005c0009t0001g0022 |
6 | HG01496.hp2 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+538dupT | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 96534855 | ||||||
| chr6:96534991 | T | G | 15 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0027 others(12): Show |
52 | HG00323.hp1 HG00544.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.655+670T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96534991 | |||||||
| chr6:96535450 | G | A | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.656-794G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96535450 | |||||||
| chr6:96535460 | A | G | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.656-784A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96535460 | |||||||
| chr6:96535706 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.656-538T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96535706 | |||||||
| chr6:96535883 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.656-361T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96535883 | |||||||
| chr6:96535962 | A | C | 1 | a0001c0002t0001g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.656-282A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96535962 | |||||||
| chr6:96536041 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(141): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.656-203C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96536041 | |||||||
| chr6:96536147 | G | T | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-97G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96536147 | |||||||
| chr6:96536207 | G | C | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.656-37G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 7/18 | chr6 | 96536207 | |||||||
| chr6:96536611 | C | T | 3 | a0001c0002t0001g0057 a0001c0002t0001g0059 a0001c0015t0001g0054 |
3 | HG02886.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.802+221C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | chr6 | 96536611 | |||||||
| chr6:96536677 | A | G | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.802+287A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | chr6 | 96536677 | |||||||
| chr6:96536973 | C | CAT | 20 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(17): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.803-389_803-388dup others(2): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr6 | 96536973 | ||||||
| chr6:96537065 | C | A | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.803-309C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | chr6 | 96537065 | |||||||
| chr6:96537137 | T | C | 30 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(27): Show |
81 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.803-237T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | chr6 | 96537137 | |||||||
| chr6:96537184 | A | G | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.803-190A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 8/18 | chr6 | 96537184 | |||||||
| chr6:96537725 | A | T | 6 | a0001c0002t0001g0012 a0001c0002t0001g0069 a0001c0002t0001g0070 others(3): Show |
10 | HG00733.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.978+176A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96537725 | |||||||
| chr6:96537850 | G | A | 1 | a0001c0001t0001g0025 | 3 | HG01257.hp2 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.978+301G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96537850 | |||||||
| chr6:96537894 | A | G | 1 | a0001c0002t0001g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.978+345A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96537894 | |||||||
| chr6:96537935 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+386G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96537935 | |||||||
| chr6:96537941 | T | C | 1 | a0001c0011t0012g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.978+392T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96537941 | |||||||
| chr6:96538016 | G | A | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.978+467G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538016 | |||||||
| chr6:96538074 | C | CT | 2 | a0001c0002t0005g0013 a0001c0002t0005g0078 |
5 | HG02486.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+526dupT | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 96538074 | ||||||
| chr6:96538083 | A | T | 20 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(17): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.978+534A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538083 | |||||||
| chr6:96538149 | G | A | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.979-482G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538149 | |||||||
| chr6:96538161 | G | A | 2 | a0001c0002t0002g0075 a0001c0004t0003g0097 |
2 | HG01081.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.979-470G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538161 | |||||||
| chr6:96538202 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG01257.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.979-429T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538202 | |||||||
| chr6:96538345 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
42 | HG00408.hp1 HG00544.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.979-286A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 9/18 | chr6 | 96538345 | |||||||
| chr6:96539301 | A | G | 1 | a0001c0002t0009g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1158+491A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539301 | |||||||
| chr6:96539315 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1158+505A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539315 | |||||||
| chr6:96539368 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1158+558C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539368 | |||||||
| chr6:96539386 | A | T | 1 | a0001c0001t0023g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1158+576A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539386 | |||||||
| chr6:96539518 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0087 others(2): Show |
10 | HG00741.hp1 HG01884.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1158+708G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539518 | |||||||
| chr6:96539749 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0041 others(2): Show |
12 | HG01167.hp2 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1159-786T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539749 | |||||||
| chr6:96539993 | C | T | 1 | a0001c0011t0012g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1159-542C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96539993 | |||||||
| chr6:96540008 | T | G | 20 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(17): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1159-527T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | chr6 | 96540008 | |||||||
| chr6:96540070 | G | GA | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
224 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1159-458dupA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 96540070 | ||||||
| chr6:96540683 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1279+28A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96540683 | |||||||
| chr6:96540820 | A | T | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(84): Show |
206 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1279+165A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96540820 | |||||||
| chr6:96541040 | C | G | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1279+385C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541040 | |||||||
| chr6:96541042 | C | T | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1279+387C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541042 | |||||||
| chr6:96541146 | C | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0066 others(12): Show |
37 | HG00408.hp1 HG00544.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1279+491C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541146 | |||||||
| chr6:96541313 | A | C | 2 | a0001c0002t0005g0013 a0001c0002t0005g0078 |
5 | HG02486.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+658A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541313 | |||||||
| chr6:96541388 | T | C | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1279+733T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541388 | |||||||
| chr6:96541435 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1279+780A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541435 | |||||||
| chr6:96541463 | A | G | 34 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(31): Show |
86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1279+808A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541463 | |||||||
| chr6:96541616 | T | TTA | 33 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(30): Show |
84 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1279+962_1279+963d others(4): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 96541616 | ||||||
| chr6:96541684 | T | C | 2 | a0001c0002t0001g0051 a0001c0002t0001g0053 |
2 | HG00597.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1279+1029T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96541684 | |||||||
| chr6:96542046 | C | T | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1280-848C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542046 | |||||||
| chr6:96542085 | T | G | 4 | a0001c0001t0006g0062 a0001c0001t0006g0063 a0001c0001t0006g0064 others(1): Show |
4 | HG01109.hp1 HG03453.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280-809T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542085 | |||||||
| chr6:96542309 | G | A | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1280-585G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542309 | |||||||
| chr6:96542318 | T | G | 34 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(31): Show |
86 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1280-576T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542318 | |||||||
| chr6:96542378 | G | GT | 2 | a0001c0001t0001g0014 a0001c0001t0001g0021 |
7 | HG00741.hp1 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-513dupT | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 96542378 | ||||||
| chr6:96542411 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1280-483G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542411 | |||||||
| chr6:96542613 | G | A | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1280-281G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542613 | |||||||
| chr6:96542635 | G | A | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1280-259G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 11/18 | chr6 | 96542635 | |||||||
| chr6:96543229 | G | A | 21 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(18): Show |
56 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1402+213G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543229 | |||||||
| chr6:96543265 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1402+249A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543265 | |||||||
| chr6:96543398 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1402+382C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543398 | |||||||
| chr6:96543489 | C | T | 4 | a0001c0011t0012g0136 a0001c0011t0012g0137 a0007c0010t0021g0094 others(1): Show |
4 | HG01891.hp1 HG02293.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402+473C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543489 | |||||||
| chr6:96543584 | A | T | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1402+568A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543584 | |||||||
| chr6:96543711 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1402+695G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543711 | |||||||
| chr6:96543982 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1402+966G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96543982 | |||||||
| chr6:96544014 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1402+998A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544014 | |||||||
| chr6:96544023 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1402+1007T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544023 | |||||||
| chr6:96544259 | C | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1402+1243C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544259 | |||||||
| chr6:96544291 | A | G | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0004g0018 others(2): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1402+1275A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544291 | |||||||
| chr6:96544352 | C | T | 8 | a0001c0002t0001g0003 a0001c0002t0001g0027 a0001c0002t0001g0045 others(5): Show |
30 | HG02015.hp1 HG02080.hp1 HG02155.hp2 others(27): Show |
intron_variant | MODIFIER | c.1402+1336C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544352 | |||||||
| chr6:96544417 | T | A | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1402+1401T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544417 | |||||||
| chr6:96544418 | T | C | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1402+1402T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544418 | |||||||
| chr6:96544476 | G | A | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1402+1460G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544476 | |||||||
| chr6:96544537 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1402+1521G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544537 | |||||||
| chr6:96544630 | G | A | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1402+1614G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544630 | |||||||
| chr6:96544761 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
7 | HG00733.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1402+1745G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544761 | |||||||
| chr6:96544953 | C | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1402+1937C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96544953 | |||||||
| chr6:96545025 | A | G | 1 | a0001c0002t0001g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1402+2009A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545025 | |||||||
| chr6:96545144 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0018g0026 |
3 | HG01081.hp1 HG01255.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1402+2128A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545144 | |||||||
| chr6:96545263 | G | A | 20 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(17): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1402+2247G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545263 | |||||||
| chr6:96545415 | G | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1402+2399G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545415 | |||||||
| chr6:96545477 | T | C | 1 | a0001c0003t0004g0032 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1402+2461T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545477 | |||||||
| chr6:96545689 | C | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(10): Show |
38 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.1403-2475C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545689 | |||||||
| chr6:96545828 | A | C | 4 | a0001c0002t0001g0012 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
7 | HG00733.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1403-2336A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545828 | |||||||
| chr6:96545849 | C | T | 1 | a0001c0011t0012g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1403-2315C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545849 | |||||||
| chr6:96545866 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1403-2298A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545866 | |||||||
| chr6:96545869 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1403-2295C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545869 | |||||||
| chr6:96545967 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1403-2197G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545967 | |||||||
| chr6:96545969 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0091 |
6 | HG02145.hp2 HG02572.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-2195A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96545969 | |||||||
| chr6:96546105 | T | G | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1403-2059T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546105 | |||||||
| chr6:96546140 | T | A | 1 | a0001c0001t0001g0010 | 5 | HG00140.hp1 HG01346.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-2024T>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546140 | |||||||
| chr6:96546275 | C | CA | 35 | a0001c0001t0001g0040 a0001c0001t0001g0112 a0001c0001t0001g0113 others(32): Show |
88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1403-1875dupA | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 96546275 | ||||||
| chr6:96546275 | CAAAA | C | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0004g0018 others(2): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1403-1878_1403-187 others(8): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 96546275 | ||||||
| chr6:96546377 | A | G | 1 | a0001c0001t0001g0023 | 3 | HG01496.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-1787A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546377 | |||||||
| chr6:96546429 | T | G | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1403-1735T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546429 | |||||||
| chr6:96546628 | A | G | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1403-1536A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546628 | |||||||
| chr6:96546732 | C | T | 4 | a0001c0003t0001g0073 a0001c0003t0004g0018 a0001c0003t0004g0032 others(1): Show |
7 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1403-1432C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546732 | |||||||
| chr6:96546877 | A | C | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1403-1287A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546877 | |||||||
| chr6:96546888 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0130 |
2 | NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1403-1276C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96546888 | |||||||
| chr6:96547016 | TCTGCACA others(4): Show |
T | 1 | a0001c0003t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1403-1147_1403-113 others(15): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547016 | |||||||
| chr6:96547075 | A | G | 1 | a0001c0011t0012g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1403-1089A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547075 | |||||||
| chr6:96547077 | A | T | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1403-1087A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547077 | |||||||
| chr6:96547181 | C | A | 1 | a0001c0002t0001g0028 | 3 | HG00735.hp1 HG01496.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1403-983C>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547181 | |||||||
| chr6:96547439 | A | G | 1 | a0001c0002t0016g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1403-725A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547439 | |||||||
| chr6:96547442 | A | G | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1403-722A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547442 | |||||||
| chr6:96547765 | G | A | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1403-399G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547765 | |||||||
| chr6:96547810 | G | T | 1 | a0001c0002t0001g0029 | 2 | HG00673.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1403-354G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547810 | |||||||
| chr6:96547811 | G | T | 1 | a0001c0002t0016g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1403-353G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547811 | |||||||
| chr6:96547812 | G | A | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1403-352G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547812 | |||||||
| chr6:96547816 | G | T | 2 | a0001c0002t0001g0144 a0001c0002t0011g0036 |
3 | HG03041.hp1 HG03579.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1403-348G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547816 | |||||||
| chr6:96547824 | G | T | 1 | a0001c0001t0006g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-340G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547824 | |||||||
| chr6:96547892 | G | C | 1 | a0001c0001t0014g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1403-272G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547892 | |||||||
| chr6:96547929 | T | C | 1 | a0001c0011t0012g0137 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1403-235T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96547929 | |||||||
| chr6:96548024 | T | G | 1 | a0004c0007t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1403-140T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96548024 | |||||||
| chr6:96548087 | T | C | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1403-77T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 12/18 | chr6 | 96548087 | |||||||
| chr6:96548352 | A | T | 20 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(17): Show |
55 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1520+71A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548352 | |||||||
| chr6:96548368 | A | G | 21 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(18): Show |
56 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1520+87A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548368 | |||||||
| chr6:96548456 | A | G | 1 | a0001c0001t0001g0043 | 2 | HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1520+175A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548456 | |||||||
| chr6:96548490 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1520+209A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548490 | |||||||
| chr6:96548591 | G | A | 1 | a0007c0010t0021g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1520+310G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548591 | |||||||
| chr6:96548834 | A | G | 1 | a0001c0002t0005g0078 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1520+553A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548834 | |||||||
| chr6:96548845 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1520+564T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548845 | |||||||
| chr6:96548957 | G | A | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(84): Show |
206 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1521-455G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96548957 | |||||||
| chr6:96549011 | ACTG | A | 1 | a0001c0001t0001g0023 | 3 | HG01496.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1521-398_1521-396d others(5): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 96549011 | ||||||
| chr6:96549137 | A | T | 1 | a0001c0002t0001g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1521-275A>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96549137 | |||||||
| chr6:96549401 | C | T | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1521-11C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 13/18 | chr6 | 96549401 | |||||||
| chr6:96550046 | T | C | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1818+247T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550046 | |||||||
| chr6:96550127 | C | G | 1 | a0001c0002t0001g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1818+328C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550127 | |||||||
| chr6:96550182 | C | T | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0004g0018 others(2): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1818+383C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550182 | |||||||
| chr6:96550276 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1818+477C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550276 | |||||||
| chr6:96550554 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1818+755T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550554 | |||||||
| chr6:96550604 | A | C | 1 | a0001c0002t0002g0077 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1818+805A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550604 | |||||||
| chr6:96550757 | A | G | 1 | a0001c0002t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1819-676A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550757 | |||||||
| chr6:96550765 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1819-668T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550765 | |||||||
| chr6:96550865 | A | G | 1 | a0007c0010t0022g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1819-568A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550865 | |||||||
| chr6:96550977 | C | T | 1 | a0001c0001t0006g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1819-456C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96550977 | |||||||
| chr6:96551070 | A | G | 1 | a0001c0002t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1819-363A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96551070 | |||||||
| chr6:96551222 | T | TGGAGCAG others(6): Show |
21 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0020 others(18): Show |
56 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1819-202_1819-190d others(15): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr6 | 96551222 | ||||||
| chr6:96551229 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1819-204G>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96551229 | |||||||
| chr6:96551311 | C | G | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1819-122C>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96551311 | |||||||
| chr6:96551344 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
334 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.1819-89G>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96551344 | |||||||
| chr6:96551387 | C | T | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0004g0018 others(2): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1819-46C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 15/18 | chr6 | 96551387 | |||||||
| chr6:96551694 | A | G | 1 | a0001c0002t0011g0036 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1900-144A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 16/18 | chr6 | 96551694 | |||||||
| chr6:96551767 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
225 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1900-71A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 16/18 | chr6 | 96551767 | |||||||
| chr6:96551779 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1900-59C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 16/18 | chr6 | 96551779 | |||||||
| chr6:96551808 | AG | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
5 | HG00597.hp2 HG02074.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900-29delG | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 16/18 | chr6 | 96551808 | |||||||
| chr6:96552029 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1985+106A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552029 | |||||||
| chr6:96552079 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1985+156T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552079 | |||||||
| chr6:96552086 | ATAGT | A | 1 | a0001c0001t0001g0021 | 3 | HG00741.hp1 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1985+167_1985+170d others(6): Show |
UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 96552086 | ||||||
| chr6:96552120 | A | G | 1 | a0001c0002t0020g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1985+197A>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552120 | |||||||
| chr6:96552194 | G | A | 2 | a0001c0011t0012g0136 a0001c0011t0012g0137 |
2 | HG01891.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1985+271G>A | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552194 | |||||||
| chr6:96552203 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1986-279C>T | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552203 | |||||||
| chr6:96552292 | T | C | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1986-190T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552292 | |||||||
| chr6:96552466 | T | C | 2 | a0007c0010t0021g0094 a0007c0010t0022g0093 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1986-16T>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 17/18 | chr6 | 96552466 | |||||||
| chr6:96552761 | A | C | 4 | a0001c0003t0001g0073 a0001c0003t0004g0018 a0001c0003t0004g0032 others(1): Show |
7 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.2166+99A>C | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 18/18 | chr6 | 96552761 | |||||||
| chr6:96552933 | T | G | 1 | a0003c0006t0007g0044 | 2 | NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2166+271T>G | UFL1 | ENSG00000014123.10 | transcript | ENST00000369278.5 | protein_coding | 18/18 | chr6 | 96552933 |