Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 144453 |
| ensemblid | ENSG00000127325.19 |
| hgncid | 17105 |
| symbol | BEST3 |
| name | bestrophin 3 |
| refseq_nuc | NM_032735.3 |
| refseq_prot | NP_116124.2 |
| ensembl_nuc | ENST00000330891.10 |
| ensembl_prot | ENSP00000332413.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 69653609 |
| end | 69699303 |
| strand | - |
| ver | v1.2 |
| region | chr12:69653609-69699303 |
| region5000 | chr12:69648609-69704303 |
| regionname0 | BEST3_chr12_69653609_69699303 |
| regionname5000 | BEST3_chr12_69648609_69704303 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 668 | 322 | 77 | 60 | 136 | 18 | 29 | 107 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0002 | 0/0 | 668 | 19 | 1 | 4 | 7 | 0 | 7 | 5 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0003 | 0/0 | 668 | 16 | 9 | 4 | 1 | 0 | 2 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0004 | 0/0 | 668 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0005 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0006 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0007 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0008 | 0/0 | 668 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| a0009 | 0/0 | 668 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | MTVTY others(663): Show |
chr12 | 69648609 | 69704303 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2004 | 306 | 64 | 59 | 136 | 17 | 29 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0001c0004 | 1/0 | 2004 | 10 | 9 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0001c0006 | 0/0 | 2004 | 4 | 4 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0001c0007 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0001c0010 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0002c0002 | 0/0 | 2004 | 19 | 1 | 4 | 7 | 0 | 7 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0003c0003 | 0/0 | 2004 | 16 | 9 | 4 | 1 | 0 | 2 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0004c0005 | 0/0 | 2004 | 4 | 4 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0005c0013 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0006c0008 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0007c0012 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0008c0009 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 | ||
| a0009c0011 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | ATGAC others(1999): Show |
chr12 | 69648609 | 69704303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3419 | 203 | 43 | 30 | 109 | 9 | 12 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0002 | 0/0 | 3419 | 60 | 6 | 13 | 23 | 5 | 13 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0003 | 0/0 | 3419 | 14 | 8 | 2 | 0 | 0 | 4 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0004 | 0/1 | 3419 | 13 | 0 | 11 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0005 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0007 | 0/0 | 3419 | 4 | 4 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0008 | 0/0 | 3419 | 2 | 0 | 2 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0009 | 0/0 | 3419 | 2 | 0 | 1 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0010 | 0/0 | 3419 | 2 | 2 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0012 | 0/0 | 3419 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0013 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0014 | 0/0 | 3419 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0001t0015 | 0/0 | 3419 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0004t0001 | 1/0 | 3419 | 8 | 7 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0004t0011 | 0/0 | 3419 | 2 | 2 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0006t0006 | 0/0 | 3419 | 4 | 4 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0007t0001 | 0/0 | 3419 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0001c0010t0001 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0002c0002t0002 | 0/0 | 3419 | 18 | 1 | 4 | 7 | 0 | 6 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0002c0002t0003 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0003c0003t0001 | 0/0 | 3419 | 16 | 9 | 4 | 1 | 0 | 2 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0004c0005t0005 | 0/0 | 3419 | 4 | 4 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0005c0013t0001 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0006c0008t0001 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0007c0012t0002 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0008c0009t0001 | 0/0 | 3419 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| a0009c0011t0002 | 0/0 | 3419 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | GACAC others(3414): Show |
chr12 | 69648609 | 69704303 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0003 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0010g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0014g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0014 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0004t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0006t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0006t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0006t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0006t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0007t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0001c0010t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0004c0005t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0004c0005t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0004c0005t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0004c0005t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0005c0013t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0006c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0007c0012t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0008c0009t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| a0009c0011t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0286 | EUR | GBR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0296 | EUR | GBR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0045 | EUR | GBR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | FIN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0046 | EUR | FIN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00423 | hp1 | a0001 | c0001 | t0014 | g0297 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0223 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0037 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0283 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0253 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01361 | hp2 | a0001 | c0007 | t0001 | g0058 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0210 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01884 | hp2 | a0004 | c0005 | t0005 | g0206 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02055 | hp1 | a0001 | c0004 | t0011 | g0061 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02055 | hp2 | a0005 | c0013 | t0001 | g0212 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | CDX | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0059 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0246 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02630 | hp2 | a0004 | c0005 | t0005 | g0213 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0236 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02922 | hp1 | a0004 | c0005 | t0005 | g0214 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0222 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0057 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0230 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03098 | hp2 | a0001 | c0006 | t0006 | g0238 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03486 | hp1 | a0001 | c0004 | t0011 | g0060 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0271 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0252 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0312 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03704 | hp1 | a0006 | c0008 | t0001 | g0124 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0241 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03831 | hp2 | a0007 | c0012 | t0002 | g0311 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0254 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0249 | SAS | STU | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18522 | hp2 | a0001 | c0006 | t0006 | g0237 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0220 | EAS | CHB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18906 | hp1 | a0001 | c0006 | t0006 | g0204 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18940 | hp2 | a0001 | c0001 | t0015 | g0182 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18964 | hp1 | a0001 | c0001 | t0012 | g0174 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18965 | hp1 | a0008 | c0009 | t0001 | g0108 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0239 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19065 | hp2 | a0009 | c0011 | t0002 | g0258 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ASW | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ASW | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20805 | hp1 | a0001 | c0010 | t0001 | g0169 | EUR | TSI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | GIH | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0209 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02486 | hp1 | a0001 | c0006 | t0006 | g0184 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0231 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG02559 | hp2 | a0004 | c0005 | t0005 | g0215 | AFR | ACB | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0056 | AFR | USA | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA18955 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | USA | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0234 | AFR | USA | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0314 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | LWK | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0041 | REF | REF | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0014 | REF | REF | BEST3_chr12_69648609_69704303 | BEST3 | chr12 | 69648609 | 69704303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69655044 | A | T | 1 | a0008 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.1870T>A | p.Ser624Thr | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1984/3419 | 1870/2007 | 624/668 | chr12 | 69655044 | |||
| chr12:69655049 | T | C | 1 | a0003 | 16 | HG01243.hp1 HG01256.hp2 HG01258.hp1 others(13): Show |
missense_variant | MODERATE | c.1865A>G | p.Glu622Gly | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1979/3419 | 1865/2007 | 622/668 | chr12 | 69655049 | |||
| chr12:69676990 | C | T | 1 | a0004 | 4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.793G>A | p.Ala265Thr | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/10 | 907/3419 | 793/2007 | 265/668 | chr12 | 69676990 | |||
| chr12:69677020 | G | A | 1 | a0009 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.763C>T | p.Arg255Cys | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/10 | 877/3419 | 763/2007 | 255/668 | chr12 | 69677020 | |||
| chr12:69677196 | G | A | 1 | a0009 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.698C>T | p.Pro233Leu | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 6/10 | 812/3419 | 698/2007 | 233/668 | chr12 | 69677196 | |||
| chr12:69693760 | A | G | 1 | a0006 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.395T>C | p.Val132Ala | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/10 | 509/3419 | 395/2007 | 132/668 | chr12 | 69693760 | |||
| chr12:69693836 | T | A | 1 | a0007 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.319A>T | p.Met107Leu | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/10 | 433/3419 | 319/2007 | 107/668 | chr12 | 69693836 | |||
| chr12:69693901 | T | G | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.254A>C | p.Tyr85Ser | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/10 | 368/3419 | 254/2007 | 85/668 | chr12 | 69693901 | |||
| chr12:69697672 | A | G | 1 | a0002 | 19 | HG00609.hp1 HG01358.hp2 HG01928.hp2 others(16): Show |
missense_variant | MODERATE | c.127T>C | p.Tyr43His | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/10 | 241/3419 | 127/2007 | 43/668 | chr12 | 69697672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69655404 | A | G | 1 | a0001c0007 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.1510T>C | p.Leu504Leu | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1624/3419 | 1510/2007 | 504/668 | chr12 | 69655404 | |||
| chr12:69655686 | T | G | 1 | a0001c0010 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1228A>C | p.Arg410Arg | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1342/3419 | 1228/2007 | 410/668 | chr12 | 69655686 | |||
| chr12:69655708 | G | A | 1 | a0001c0006 | 4 | HG02486.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.1206C>T | p.His402His | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1320/3419 | 1206/2007 | 402/668 | chr12 | 69655708 | |||
| chr12:69697652 | T | C | 11 | a0001c0001 a0001c0006 a0001c0010 others(8): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
synonymous_variant | LOW | c.147A>G | p.Val49Val | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/10 | 261/3419 | 147/2007 | 49/668 | chr12 | 69697652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69653614 | T | C | 1 | a0001c0001t0007 | 4 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1293A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1293 | chr12 | 69653614 | ||||||
| chr12:69653672 | G | A | 1 | a0001c0004t0011 | 2 | HG02055.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1235C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1235 | chr12 | 69653672 | ||||||
| chr12:69653718 | C | T | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0013 |
15 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1189G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1189 | chr12 | 69653718 | ||||||
| chr12:69653789 | C | A | 1 | a0001c0001t0015 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1118 | chr12 | 69653789 | ||||||
| chr12:69653836 | G | A | 2 | a0001c0001t0005 a0004c0005t0005 |
5 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1071C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 1071 | chr12 | 69653836 | ||||||
| chr12:69653936 | G | A | 1 | a0001c0001t0014 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*971C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 971 | chr12 | 69653936 | ||||||
| chr12:69653973 | G | C | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(3): Show |
37 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*934C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 934 | chr12 | 69653973 | ||||||
| chr12:69654055 | C | G | 1 | a0001c0001t0012 | 2 | NA18955.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*852G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 852 | chr12 | 69654055 | ||||||
| chr12:69654067 | C | T | 1 | a0001c0001t0009 | 2 | HG00140.hp2 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*840G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 840 | chr12 | 69654067 | ||||||
| chr12:69654239 | C | G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(8): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*668G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 668 | chr12 | 69654239 | ||||||
| chr12:69654248 | C | A | 1 | a0001c0001t0007 | 4 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 659 | chr12 | 69654248 | ||||||
| chr12:69654405 | G | T | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(5): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*502C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 502 | chr12 | 69654405 | ||||||
| chr12:69654429 | G | A | 1 | a0001c0001t0007 | 4 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*478C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 478 | chr12 | 69654429 | ||||||
| chr12:69654586 | A | C | 1 | a0001c0001t0010 | 2 | NA19043.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*321T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 321 | chr12 | 69654586 | ||||||
| chr12:69654714 | G | A | 1 | a0001c0001t0007 | 4 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*193C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 10/10 | 193 | chr12 | 69654714 | ||||||
| chr12:69699255 | G | T | 3 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-66C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/10 | 1457 | chr12 | 69699255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69655853 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1101-40C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69655853 | |||||||
| chr12:69655980 | C | T | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-167G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69655980 | |||||||
| chr12:69656014 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
78 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1101-201C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656014 | |||||||
| chr12:69656087 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1101-274A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656087 | |||||||
| chr12:69656122 | G | A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
11 | HG01167.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101-309C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656122 | |||||||
| chr12:69656369 | A | ATCTG | 244 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1101-560_1101-557d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656369 | |||||||
| chr12:69656381 | G | GTCTGTCT others(5): Show |
1 | a0001c0006t0006g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101-569_1101-568i others(14): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656381 | |||||||
| chr12:69656482 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1101-669G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656482 | |||||||
| chr12:69656495 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1101-682C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656495 | |||||||
| chr12:69656539 | T | C | 2 | a0001c0004t0011g0060 a0001c0004t0011g0061 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1101-726A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656539 | |||||||
| chr12:69656630 | A | T | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-817T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656630 | |||||||
| chr12:69656825 | A | C | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-1012T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656825 | |||||||
| chr12:69656828 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1101-1015C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656828 | |||||||
| chr12:69656878 | G | A | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-1065C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69656878 | |||||||
| chr12:69657038 | A | G | 1 | a0001c0001t0014g0297 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1101-1225T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657038 | |||||||
| chr12:69657164 | C | T | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1101-1351G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657164 | |||||||
| chr12:69657357 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1101-1544T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657357 | |||||||
| chr12:69657688 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | NA18949.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1101-1875T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657688 | |||||||
| chr12:69657816 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1101-2003A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657816 | |||||||
| chr12:69657881 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1101-2068T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69657881 | |||||||
| chr12:69658128 | A | T | 79 | a0001c0001t0001g0285 a0001c0001t0001g0300 a0001c0001t0002g0012 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1101-2315T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658128 | |||||||
| chr12:69658455 | T | C | 1 | a0001c0001t0001g0011 | 3 | HG02451.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1101-2642A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658455 | |||||||
| chr12:69658668 | G | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
78 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1101-2855C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658668 | |||||||
| chr12:69658874 | G | A | 77 | a0001c0001t0001g0285 a0001c0001t0001g0300 a0001c0001t0002g0012 others(74): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1101-3061C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658874 | |||||||
| chr12:69658906 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(220): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1101-3093G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658906 | |||||||
| chr12:69658988 | G | A | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-3175C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69658988 | |||||||
| chr12:69659032 | A | G | 2 | a0001c0004t0011g0060 a0001c0004t0011g0061 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1101-3219T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659032 | |||||||
| chr12:69659083 | AG | A | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1101-3271delC | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659083 | |||||||
| chr12:69659111 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1101-3298C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659111 | |||||||
| chr12:69659116 | C | A | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1101-3303G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659116 | |||||||
| chr12:69659357 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1101-3544T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659357 | |||||||
| chr12:69659407 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0273 |
2 | HG03491.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1101-3594C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659407 | |||||||
| chr12:69659465 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1101-3652G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659465 | |||||||
| chr12:69659492 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1101-3679G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659492 | |||||||
| chr12:69659717 | T | TG | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1101-3905_1101-390 others(5): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659717 | |||||||
| chr12:69659718 | T | G | 1 | a0002c0002t0002g0251 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1101-3905A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659718 | |||||||
| chr12:69659902 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1101-4089C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659902 | |||||||
| chr12:69659961 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1101-4148T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659961 | |||||||
| chr12:69659973 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1101-4160G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69659973 | |||||||
| chr12:69660167 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0075 |
3 | NA18971.hp2 NA18980.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1101-4354C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660167 | |||||||
| chr12:69660261 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1101-4448T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660261 | |||||||
| chr12:69660290 | T | C | 1 | a0001c0001t0007g0236 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1101-4477A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660290 | |||||||
| chr12:69660323 | A | G | 1 | a0001c0001t0010g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1101-4510T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660323 | |||||||
| chr12:69660375 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1101-4562T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660375 | |||||||
| chr12:69660391 | G | T | 2 | a0001c0001t0010g0239 a0001c0001t0010g0314 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1101-4578C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660391 | |||||||
| chr12:69660693 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1101-4880G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660693 | |||||||
| chr12:69660988 | A | G | 19 | a0001c0001t0001g0300 a0001c0001t0002g0012 a0001c0001t0002g0269 others(16): Show |
21 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1101-5175T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69660988 | |||||||
| chr12:69661130 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
81 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1101-5317T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661130 | |||||||
| chr12:69661246 | T | C | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1101-5433A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661246 | |||||||
| chr12:69661302 | G | A | 79 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0300 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1101-5489C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661302 | |||||||
| chr12:69661318 | T | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1101-5505A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661318 | |||||||
| chr12:69661337 | C | G | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-5524G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661337 | |||||||
| chr12:69661357 | T | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
83 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1101-5544A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661357 | |||||||
| chr12:69661434 | T | A | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1101-5621A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661434 | |||||||
| chr12:69661472 | T | A | 2 | a0001c0004t0011g0060 a0001c0004t0011g0061 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1101-5659A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661472 | |||||||
| chr12:69661536 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1101-5723C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661536 | |||||||
| chr12:69661538 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1101-5725T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661538 | |||||||
| chr12:69661812 | C | T | 79 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0300 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1101-5999G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661812 | |||||||
| chr12:69661832 | G | C | 2 | a0001c0001t0010g0239 a0001c0001t0010g0314 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1101-6019C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661832 | |||||||
| chr12:69661870 | G | T | 1 | a0001c0006t0006g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101-6057C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661870 | |||||||
| chr12:69661944 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1101-6131A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69661944 | |||||||
| chr12:69662005 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1101-6192G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662005 | |||||||
| chr12:69662016 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1101-6203T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662016 | |||||||
| chr12:69662058 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1101-6245A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662058 | |||||||
| chr12:69662085 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
82 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1101-6272T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662085 | |||||||
| chr12:69662123 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1101-6310C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662123 | |||||||
| chr12:69662131 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1101-6318C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662131 | |||||||
| chr12:69662198 | T | C | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-6385A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662198 | |||||||
| chr12:69662214 | C | T | 1 | a0003c0003t0001g0230 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1101-6401G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662214 | |||||||
| chr12:69662295 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1101-6482C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662295 | |||||||
| chr12:69662329 | C | T | 1 | a0003c0003t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1101-6516G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662329 | |||||||
| chr12:69662437 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1101-6624A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662437 | |||||||
| chr12:69662473 | T | C | 3 | a0001c0006t0006g0184 a0001c0006t0006g0204 a0001c0006t0006g0237 |
3 | HG02486.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1101-6660A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662473 | |||||||
| chr12:69662485 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1101-6672A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662485 | |||||||
| chr12:69662558 | A | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1101-6745T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662558 | |||||||
| chr12:69662735 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1101-6922C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662735 | |||||||
| chr12:69662913 | C | A | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1101-7100G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662913 | |||||||
| chr12:69662991 | A | T | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1101-7178T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69662991 | |||||||
| chr12:69663020 | A | G | 1 | a0001c0006t0006g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1101-7207T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663020 | |||||||
| chr12:69663022 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1101-7209C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663022 | |||||||
| chr12:69663024 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1101-7211G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663024 | |||||||
| chr12:69663054 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1101-7241C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663054 | |||||||
| chr12:69663078 | TAA | T | 3 | a0003c0003t0001g0033 a0003c0003t0001g0229 a0003c0003t0001g0230 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101-7267_1101-726 others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663078 | |||||||
| chr12:69663287 | T | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1101-7474A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663287 | |||||||
| chr12:69663636 | G | T | 2 | a0001c0001t0001g0199 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1100+7792C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663636 | |||||||
| chr12:69663826 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1100+7602T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663826 | |||||||
| chr12:69663836 | G | A | 79 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0300 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1100+7592C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69663836 | |||||||
| chr12:69664022 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1100+7406C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664022 | |||||||
| chr12:69664042 | A | T | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100+7386T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664042 | |||||||
| chr12:69664080 | A | C | 18 | a0001c0001t0001g0199 a0001c0001t0003g0031 a0001c0001t0003g0055 others(15): Show |
19 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1100+7348T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664080 | |||||||
| chr12:69664094 | G | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0097 others(13): Show |
21 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1100+7334C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664094 | |||||||
| chr12:69664097 | T | A | 1 | a0002c0002t0002g0242 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1100+7331A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664097 | |||||||
| chr12:69664111 | T | C | 3 | a0001c0001t0002g0270 a0001c0001t0002g0276 a0001c0001t0002g0296 |
3 | HG00140.hp1 HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1100+7317A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664111 | |||||||
| chr12:69664118 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1100+7310G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664118 | |||||||
| chr12:69664176 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1100+7252T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664176 | |||||||
| chr12:69664185 | C | A | 2 | a0001c0001t0001g0199 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1100+7243G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664185 | |||||||
| chr12:69664186 | G | A | 3 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1100+7242C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664186 | |||||||
| chr12:69664225 | G | A | 13 | a0001c0001t0003g0031 a0001c0001t0003g0055 a0001c0001t0003g0185 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100+7203C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664225 | |||||||
| chr12:69664252 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+7176G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664252 | |||||||
| chr12:69664386 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18947.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1100+7042T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664386 | |||||||
| chr12:69664439 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+6989G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664439 | |||||||
| chr12:69664457 | A | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1100+6971T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664457 | |||||||
| chr12:69664478 | G | C | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100+6950C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664478 | |||||||
| chr12:69664481 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1100+6947T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664481 | |||||||
| chr12:69664518 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1100+6910C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664518 | |||||||
| chr12:69664554 | T | C | 2 | a0001c0006t0006g0204 a0001c0006t0006g0237 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1100+6874A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664554 | |||||||
| chr12:69664646 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1100+6782T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664646 | |||||||
| chr12:69664690 | A | C | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100+6738T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664690 | |||||||
| chr12:69664694 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1100+6734T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664694 | |||||||
| chr12:69664706 | AAT | A | 3 | a0001c0001t0001g0308 a0001c0001t0010g0239 a0001c0006t0006g0238 |
3 | HG02818.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1100+6720_1100+672 others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664706 | |||||||
| chr12:69664824 | G | T | 1 | a0006c0008t0001g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1100+6604C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664824 | |||||||
| chr12:69664919 | C | A | 18 | a0001c0001t0002g0166 a0001c0001t0002g0260 a0002c0002t0002g0034 others(15): Show |
20 | HG00609.hp1 HG01358.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1100+6509G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664919 | |||||||
| chr12:69664919 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1100+6509G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69664919 | |||||||
| chr12:69665000 | C | CTAAAAGG others(102): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
7 | HG00639.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100+6319_1100+642 others(113): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665000 | |||||||
| chr12:69665000 | CTAAAAGG others(102): Show |
C | 92 | a0001c0001t0001g0201 a0001c0001t0001g0282 a0001c0001t0001g0285 others(89): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1100+6319_1100+642 others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665000 | |||||||
| chr12:69665016 | G | GTCACACA others(102): Show |
1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1100+6411_1100+641 others(113): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665016 | |||||||
| chr12:69665033 | ACTACAGC others(211): Show |
A | 1 | a0002c0002t0003g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100+6177_1100+639 others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665033 | |||||||
| chr12:69665125 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1100+6303C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665125 | |||||||
| chr12:69665142 | ACTACAGC others(102): Show |
A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0096 others(2): Show |
5 | HG02027.hp1 HG02056.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100+6177_1100+628 others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665142 | |||||||
| chr12:69665256 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1100+6172T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665256 | |||||||
| chr12:69665279 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1100+6149T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665279 | |||||||
| chr12:69665501 | G | A | 7 | a0001c0001t0001g0313 a0001c0001t0005g0203 a0001c0001t0007g0236 others(4): Show |
7 | HG00741.hp1 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100+5927C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665501 | |||||||
| chr12:69665502 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
11 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1100+5926C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665502 | |||||||
| chr12:69665563 | A | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5865T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665563 | |||||||
| chr12:69665608 | CACAAAAA others(5): Show |
C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5808_1100+581 others(16): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665608 | |||||||
| chr12:69665662 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5766A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665662 | |||||||
| chr12:69665663 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5765C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665663 | |||||||
| chr12:69665832 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1100+5596C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665832 | |||||||
| chr12:69665946 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1100+5482C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665946 | |||||||
| chr12:69665958 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1100+5470A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665958 | |||||||
| chr12:69665964 | T | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1100+5464A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665964 | |||||||
| chr12:69665986 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1100+5442A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69665986 | |||||||
| chr12:69666023 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0088 others(13): Show |
18 | HG02083.hp2 HG02148.hp1 NA18948.hp1 others(15): Show |
intron_variant | MODIFIER | c.1100+5405G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666023 | |||||||
| chr12:69666047 | T | G | 2 | a0001c0001t0012g0147 a0001c0001t0012g0174 |
2 | NA18955.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1100+5381A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666047 | |||||||
| chr12:69666113 | G | T | 1 | a0001c0010t0001g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1100+5315C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666113 | |||||||
| chr12:69666146 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1100+5282T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666146 | |||||||
| chr12:69666246 | G | A | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1100+5182C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666246 | |||||||
| chr12:69666298 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5130C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666298 | |||||||
| chr12:69666318 | C | T | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1100+5110G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666318 | |||||||
| chr12:69666319 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100+5109C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666319 | |||||||
| chr12:69666502 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1100+4926G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666502 | |||||||
| chr12:69666573 | G | A | 14 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1100+4855C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666573 | |||||||
| chr12:69666597 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(21): Show |
28 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1100+4831G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666597 | |||||||
| chr12:69666643 | G | A | 1 | a0001c0006t0006g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1100+4785C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666643 | |||||||
| chr12:69666883 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1100+4545A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666883 | |||||||
| chr12:69666994 | C | T | 1 | a0001c0001t0010g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1100+4434G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69666994 | |||||||
| chr12:69667006 | G | T | 38 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0112 others(35): Show |
42 | HG00733.hp1 HG01070.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1100+4422C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667006 | |||||||
| chr12:69667236 | A | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1100+4192T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667236 | |||||||
| chr12:69667363 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1100+4065G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667363 | |||||||
| chr12:69667515 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1100+3913G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667515 | |||||||
| chr12:69667612 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1100+3816C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667612 | |||||||
| chr12:69667774 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1100+3654C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667774 | |||||||
| chr12:69667808 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1100+3620G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667808 | |||||||
| chr12:69667840 | T | C | 14 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1100+3588A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667840 | |||||||
| chr12:69667846 | C | G | 1 | a0001c0001t0010g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1100+3582G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69667846 | |||||||
| chr12:69668120 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1100+3308C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668120 | |||||||
| chr12:69668151 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1100+3277A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668151 | |||||||
| chr12:69668539 | C | G | 1 | a0002c0002t0002g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1100+2889G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668539 | |||||||
| chr12:69668564 | A | G | 2 | a0001c0001t0001g0199 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1100+2864T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668564 | |||||||
| chr12:69668765 | C | T | 1 | a0001c0001t0010g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1100+2663G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668765 | |||||||
| chr12:69668766 | C | T | 1 | a0001c0001t0010g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1100+2662G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668766 | |||||||
| chr12:69668860 | A | G | 3 | a0001c0001t0001g0308 a0001c0001t0010g0239 a0001c0006t0006g0238 |
3 | HG02818.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1100+2568T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668860 | |||||||
| chr12:69668914 | G | A | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1100+2514C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69668914 | |||||||
| chr12:69669000 | G | C | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1100+2428C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669000 | |||||||
| chr12:69669065 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | NA18950.hp1 NA18997.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1100+2363C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669065 | |||||||
| chr12:69669161 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0143 a0001c0001t0001g0153 |
4 | HG00423.hp2 NA18971.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100+2267T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669161 | |||||||
| chr12:69669229 | G | A | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1100+2199C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669229 | |||||||
| chr12:69669381 | C | T | 1 | a0001c0001t0004g0042 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1100+2047G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669381 | |||||||
| chr12:69669582 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1100+1846A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669582 | |||||||
| chr12:69669704 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1100+1724T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669704 | |||||||
| chr12:69669861 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1100+1567C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69669861 | |||||||
| chr12:69670024 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+1404T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670024 | |||||||
| chr12:69670025 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+1403C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670025 | |||||||
| chr12:69670027 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+1401A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670027 | |||||||
| chr12:69670033 | G | A | 3 | a0001c0006t0006g0184 a0001c0006t0006g0204 a0001c0006t0006g0237 |
3 | HG02486.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1100+1395C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670033 | |||||||
| chr12:69670095 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
13 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1100+1333G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670095 | |||||||
| chr12:69670158 | G | A | 82 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(79): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1100+1270C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670158 | |||||||
| chr12:69670190 | A | G | 83 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1100+1238T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670190 | |||||||
| chr12:69670213 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
13 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1100+1215T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670213 | |||||||
| chr12:69670292 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1100+1136C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670292 | |||||||
| chr12:69670366 | T | C | 83 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1100+1062A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670366 | |||||||
| chr12:69670438 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1100+990A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670438 | |||||||
| chr12:69670476 | G | A | 1 | a0001c0004t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1100+952C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670476 | |||||||
| chr12:69670515 | C | T | 83 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1100+913G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670515 | |||||||
| chr12:69670521 | A | G | 1 | a0001c0001t0004g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1100+907T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670521 | |||||||
| chr12:69670571 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1100+857C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670571 | |||||||
| chr12:69670590 | A | G | 1 | a0001c0010t0001g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1100+838T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670590 | |||||||
| chr12:69670650 | G | T | 2 | a0001c0006t0006g0204 a0001c0006t0006g0237 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1100+778C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670650 | |||||||
| chr12:69670674 | G | A | 3 | a0001c0006t0006g0184 a0001c0006t0006g0204 a0001c0006t0006g0237 |
3 | HG02486.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1100+754C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670674 | |||||||
| chr12:69670761 | G | GT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1100+666dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670761 | |||||||
| chr12:69670764 | T | TTTTTG | 12 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
15 | HG00639.hp1 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1100+659_1100+663d others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69670764 | |||||||
| chr12:69671012 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1100+416C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69671012 | |||||||
| chr12:69671292 | A | G | 83 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1100+136T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69671292 | |||||||
| chr12:69671346 | CT | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1100+81delA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69671346 | |||||||
| chr12:69671346 | CTT | C | 83 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1100+80_1100+81del others(2): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 9/9 | chr12 | 69671346 | |||||||
| chr12:69671664 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
10 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.949-85A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671664 | |||||||
| chr12:69671705 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.949-126G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671705 | |||||||
| chr12:69671727 | C | A | 1 | a0004c0005t0005g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.949-148G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671727 | |||||||
| chr12:69671817 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.949-238G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671817 | |||||||
| chr12:69671846 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.949-267C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671846 | |||||||
| chr12:69671894 | A | C | 13 | a0001c0001t0003g0031 a0001c0001t0003g0055 a0001c0001t0003g0185 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.949-315T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671894 | |||||||
| chr12:69671915 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.949-336G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69671915 | |||||||
| chr12:69672059 | A | G | 1 | a0001c0006t0006g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.949-480T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672059 | |||||||
| chr12:69672085 | A | G | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.949-506T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672085 | |||||||
| chr12:69672275 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.948+610C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672275 | |||||||
| chr12:69672278 | A | G | 3 | a0001c0006t0006g0184 a0001c0006t0006g0204 a0001c0006t0006g0237 |
3 | HG02486.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.948+607T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672278 | |||||||
| chr12:69672387 | T | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.948+498A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672387 | |||||||
| chr12:69672412 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.948+473A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672412 | |||||||
| chr12:69672433 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948+452C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672433 | |||||||
| chr12:69672500 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.948+385T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672500 | |||||||
| chr12:69672713 | G | A | 5 | a0001c0001t0005g0203 a0004c0005t0005g0206 a0004c0005t0005g0213 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+172C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672713 | |||||||
| chr12:69672867 | A | G | 6 | a0001c0001t0001g0125 a0001c0001t0001g0134 a0001c0001t0001g0159 others(3): Show |
6 | NA18954.hp1 NA18974.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.948+18T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 8/9 | chr12 | 69672867 | |||||||
| chr12:69673076 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.868-111G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673076 | |||||||
| chr12:69673081 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.868-116T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673081 | |||||||
| chr12:69673223 | G | A | 3 | a0001c0006t0006g0184 a0001c0006t0006g0204 a0001c0006t0006g0237 |
3 | HG02486.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.868-258C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673223 | |||||||
| chr12:69673417 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.868-452T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673417 | |||||||
| chr12:69673583 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.868-618C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673583 | |||||||
| chr12:69673590 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.868-625T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673590 | |||||||
| chr12:69673642 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.868-677G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673642 | |||||||
| chr12:69673659 | G | T | 2 | a0001c0001t0001g0199 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.868-694C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673659 | |||||||
| chr12:69673738 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.868-773A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673738 | |||||||
| chr12:69673743 | C | T | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.868-778G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673743 | |||||||
| chr12:69673830 | GT | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.868-866delA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673830 | |||||||
| chr12:69673879 | C | T | 2 | a0001c0001t0001g0199 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.868-914G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673879 | |||||||
| chr12:69673986 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.868-1021C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69673986 | |||||||
| chr12:69674005 | T | C | 1 | a0002c0002t0002g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.868-1040A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674005 | |||||||
| chr12:69674057 | G | A | 4 | a0001c0001t0001g0308 a0001c0001t0010g0239 a0001c0006t0006g0238 others(1): Show |
4 | HG02055.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1092C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674057 | |||||||
| chr12:69674073 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.868-1108C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674073 | |||||||
| chr12:69674102 | T | C | 8 | a0001c0001t0001g0313 a0001c0001t0007g0208 a0001c0001t0007g0209 others(5): Show |
8 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-1137A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674102 | |||||||
| chr12:69674370 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.868-1405C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674370 | |||||||
| chr12:69674439 | G | A | 4 | a0001c0004t0001g0015 a0001c0004t0001g0062 a0001c0004t0011g0060 others(1): Show |
5 | HG02055.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-1474C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674439 | |||||||
| chr12:69674599 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.868-1634G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674599 | |||||||
| chr12:69674652 | G | A | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.868-1687C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674652 | |||||||
| chr12:69674805 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.868-1840C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674805 | |||||||
| chr12:69674844 | T | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.868-1879A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674844 | |||||||
| chr12:69674892 | C | CT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(53): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.868-1928dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674892 | |||||||
| chr12:69674892 | C | CTT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(19): Show |
27 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.868-1929_868-1928d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674892 | |||||||
| chr12:69674892 | CT | C | 31 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0001g0128 others(28): Show |
32 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.868-1928delA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674892 | |||||||
| chr12:69674892 | CTT | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
119 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.868-1929_868-1928d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674892 | |||||||
| chr12:69674892 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0308 a0001c0001t0010g0239 a0001c0006t0006g0238 others(1): Show |
4 | HG02055.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1940_868-1928d others(15): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674892 | |||||||
| chr12:69674959 | T | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.867+1957A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674959 | |||||||
| chr12:69674959 | T | G | 1 | a0001c0004t0001g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867+1957A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674959 | |||||||
| chr12:69674967 | G | A | 81 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(78): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.867+1949C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69674967 | |||||||
| chr12:69675043 | G | A | 81 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0285 others(78): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.867+1873C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675043 | |||||||
| chr12:69675046 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.867+1870A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675046 | |||||||
| chr12:69675077 | T | C | 1 | a0001c0001t0002g0305 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.867+1839A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675077 | |||||||
| chr12:69675156 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0157 |
2 | NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.867+1760C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675156 | |||||||
| chr12:69675269 | G | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
12 | HG00733.hp1 HG01070.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.867+1647C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675269 | |||||||
| chr12:69675318 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.867+1598G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675318 | |||||||
| chr12:69675509 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
159 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.867+1407T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675509 | |||||||
| chr12:69675667 | G | A | 21 | a0001c0001t0002g0166 a0002c0002t0002g0034 a0002c0002t0002g0035 others(18): Show |
24 | HG00609.hp1 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.867+1249C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675667 | |||||||
| chr12:69675691 | C | T | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.867+1225G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675691 | |||||||
| chr12:69675800 | A | AT | 15 | a0001c0001t0001g0018 a0001c0001t0002g0195 a0001c0001t0003g0031 others(12): Show |
17 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+1115dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675800 | |||||||
| chr12:69675839 | G | A | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.867+1077C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675839 | |||||||
| chr12:69675839 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.867+1077C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675839 | |||||||
| chr12:69675881 | G | A | 2 | a0001c0006t0006g0184 a0001c0006t0006g0237 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.867+1035C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69675881 | |||||||
| chr12:69676119 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.867+797T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676119 | |||||||
| chr12:69676264 | A | T | 1 | a0001c0001t0001g0017 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.867+652T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676264 | |||||||
| chr12:69676279 | G | A | 2 | a0001c0006t0006g0184 a0001c0006t0006g0237 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.867+637C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676279 | |||||||
| chr12:69676367 | C | T | 3 | a0001c0001t0003g0055 a0001c0001t0003g0192 a0001c0001t0003g0193 |
3 | HG02735.hp2 HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.867+549G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676367 | |||||||
| chr12:69676419 | T | TA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.867+496dupT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676419 | |||||||
| chr12:69676419 | T | TAA | 7 | a0001c0001t0001g0122 a0001c0001t0001g0308 a0001c0001t0003g0207 others(4): Show |
7 | HG02055.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.867+495_867+496dup others(2): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676419 | |||||||
| chr12:69676508 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.867+408T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676508 | |||||||
| chr12:69676524 | T | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.867+392A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676524 | |||||||
| chr12:69676738 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.867+178G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676738 | |||||||
| chr12:69676839 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.867+77T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 7/9 | chr12 | 69676839 | |||||||
| chr12:69677081 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 |
5 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-13C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 6/9 | chr12 | 69677081 | |||||||
| chr12:69677113 | C | T | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-45G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 6/9 | chr12 | 69677113 | |||||||
| chr12:69677114 | G | A | 8 | a0001c0001t0007g0208 a0001c0001t0007g0209 a0001c0001t0007g0210 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-46C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 6/9 | chr12 | 69677114 | |||||||
| chr12:69677162 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.714+18T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 6/9 | chr12 | 69677162 | |||||||
| chr12:69677266 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.637-9C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677266 | |||||||
| chr12:69677298 | G | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(9): Show |
14 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-41C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677298 | |||||||
| chr12:69677667 | G | A | 2 | a0001c0006t0006g0184 a0001c0006t0006g0237 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-410C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677667 | |||||||
| chr12:69677733 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
95 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.637-476T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677733 | |||||||
| chr12:69677790 | A | G | 9 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-533T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677790 | |||||||
| chr12:69677974 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.637-717G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69677974 | |||||||
| chr12:69678080 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+659C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678080 | |||||||
| chr12:69678117 | T | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.636+622A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678117 | |||||||
| chr12:69678163 | A | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.636+576T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678163 | |||||||
| chr12:69678228 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+511A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678228 | |||||||
| chr12:69678232 | A | AT | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+506dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678232 | |||||||
| chr12:69678241 | A | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+498T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678241 | |||||||
| chr12:69678272 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.636+467T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678272 | |||||||
| chr12:69678277 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+462A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678277 | |||||||
| chr12:69678307 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.636+432A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678307 | |||||||
| chr12:69678313 | G | T | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.636+426C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678313 | |||||||
| chr12:69678526 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.636+213C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678526 | |||||||
| chr12:69678699 | C | G | 94 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(91): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.636+40G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 5/9 | chr12 | 69678699 | |||||||
| chr12:69679078 | T | G | 2 | a0001c0001t0003g0207 a0001c0001t0010g0314 |
2 | HG02886.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.482-185A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679078 | |||||||
| chr12:69679136 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.482-243C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679136 | |||||||
| chr12:69679349 | G | C | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.482-456C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679349 | |||||||
| chr12:69679393 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.482-500G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679393 | |||||||
| chr12:69679408 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.482-515A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679408 | |||||||
| chr12:69679438 | A | C | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-545T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679438 | |||||||
| chr12:69679514 | A | G | 2 | a0001c0006t0006g0184 a0001c0006t0006g0237 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.482-621T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679514 | |||||||
| chr12:69679578 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
117 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.482-685A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679578 | |||||||
| chr12:69679599 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.482-706C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679599 | |||||||
| chr12:69679719 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.482-826C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679719 | |||||||
| chr12:69679731 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.482-838G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679731 | |||||||
| chr12:69679750 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.482-857C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679750 | |||||||
| chr12:69679763 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0072 others(1): Show |
5 | NA18950.hp2 NA18971.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-870T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679763 | |||||||
| chr12:69679838 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.482-945C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679838 | |||||||
| chr12:69679862 | T | A | 2 | a0001c0006t0006g0184 a0001c0006t0006g0237 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.482-969A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679862 | |||||||
| chr12:69679863 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.482-970C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679863 | |||||||
| chr12:69679868 | A | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0138 a0001c0001t0001g0144 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-975T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679868 | |||||||
| chr12:69679884 | G | GGT | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-993_482-992dup others(2): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679884 | |||||||
| chr12:69679907 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
9 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-1014T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679907 | |||||||
| chr12:69679914 | C | CGT | 36 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0097 others(33): Show |
41 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.482-1023_482-1022d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679914 | |||||||
| chr12:69679914 | C | CGTGT | 85 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0199 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.482-1025_482-1022d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679914 | |||||||
| chr12:69679914 | CGT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.482-1023_482-1022d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679914 | |||||||
| chr12:69679914 | CGTGT | C | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0002g0165 others(4): Show |
7 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-1025_482-1022d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679914 | |||||||
| chr12:69679935 | G | A | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.482-1042C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679935 | |||||||
| chr12:69679957 | G | A | 28 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(25): Show |
29 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-1064C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679957 | |||||||
| chr12:69679961 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02630.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.482-1068C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69679961 | |||||||
| chr12:69680081 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.482-1188G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680081 | |||||||
| chr12:69680151 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.482-1258T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680151 | |||||||
| chr12:69680195 | T | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | NA18957.hp2 NA18965.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.482-1302A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680195 | |||||||
| chr12:69680268 | T | C | 28 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(25): Show |
29 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-1375A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680268 | |||||||
| chr12:69680310 | C | CTTCTT | 7 | a0001c0001t0002g0280 a0001c0001t0003g0187 a0001c0001t0007g0236 others(4): Show |
7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTT | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(8): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT | 15 | a0001c0001t0001g0092 a0001c0001t0004g0040 a0001c0001t0004g0042 others(12): Show |
15 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(9): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(1): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
57 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(10): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(3): Show |
1 | a0001c0006t0006g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.482-1418_482-1417i others(12): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(10): Show |
26 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0201 others(23): Show |
29 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(19): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(11): Show |
51 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0219 others(48): Show |
59 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(20): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(12): Show |
21 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0285 others(18): Show |
22 | HG00423.hp1 HG00609.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(21): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(13): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0228 a0001c0001t0002g0275 others(3): Show |
7 | HG01099.hp2 HG01167.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(22): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(14): Show |
7 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0267 others(4): Show |
7 | HG01361.hp1 HG02135.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(23): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(15): Show |
3 | a0001c0001t0001g0300 a0001c0001t0002g0303 a0001c0001t0002g0304 |
3 | HG00280.hp1 HG02300.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.482-1418_482-1417i others(24): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(17): Show |
2 | a0001c0001t0002g0302 a0001c0004t0001g0059 |
2 | HG02451.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.482-1418_482-1417i others(26): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(20): Show |
1 | a0001c0004t0001g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.482-1418_482-1417i others(29): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(21): Show |
4 | a0001c0004t0001g0015 a0001c0004t0011g0060 a0001c0004t0011g0061 others(1): Show |
5 | HG01361.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1418_482-1417i others(30): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(24): Show |
2 | a0001c0001t0007g0208 a0001c0001t0007g0209 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.482-1418_482-1417i others(33): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(25): Show |
1 | a0001c0001t0007g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482-1418_482-1417i others(34): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680310 | C | CTTCTTTT others(26): Show |
1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-1418_482-1417i others(35): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680310 | |||||||
| chr12:69680311 | T | TTCTTC | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
115 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.482-1419_482-1418i others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680311 | |||||||
| chr12:69680312 | T | TC | 7 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
9 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-1420_482-1419i others(3): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680312 | |||||||
| chr12:69680355 | C | T | 1 | a0002c0002t0002g0251 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.482-1462G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680355 | |||||||
| chr12:69680370 | G | A | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1477C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680370 | |||||||
| chr12:69680383 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.482-1490T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680383 | |||||||
| chr12:69680409 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.482-1516C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680409 | |||||||
| chr12:69680476 | G | T | 28 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(25): Show |
29 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-1583C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680476 | |||||||
| chr12:69680510 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0081 others(6): Show |
11 | NA18945.hp2 NA18957.hp1 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-1617T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680510 | |||||||
| chr12:69680523 | T | TG | 12 | a0001c0001t0001g0024 a0001c0001t0001g0112 a0001c0001t0001g0113 others(9): Show |
13 | HG00423.hp1 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.482-1631dupC | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680523 | |||||||
| chr12:69680529 | A | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
12 | HG00733.hp1 HG01070.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-1636T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680529 | |||||||
| chr12:69680549 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.482-1656G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680549 | |||||||
| chr12:69680712 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-1819T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680712 | |||||||
| chr12:69680769 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-1876T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680769 | |||||||
| chr12:69680841 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.482-1948A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680841 | |||||||
| chr12:69680941 | TAATA | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-2052_482-2049d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69680941 | |||||||
| chr12:69681020 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482-2127A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681020 | |||||||
| chr12:69681027 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-2134C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681027 | |||||||
| chr12:69681079 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-2186A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681079 | |||||||
| chr12:69681130 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-2237C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681130 | |||||||
| chr12:69681180 | G | GT | 17 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0004g0040 others(14): Show |
18 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.482-2288dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681180 | |||||||
| chr12:69681242 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.482-2349T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681242 | |||||||
| chr12:69681256 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.482-2363G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681256 | |||||||
| chr12:69681290 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-2397C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681290 | |||||||
| chr12:69681463 | A | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-2570T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681463 | |||||||
| chr12:69681607 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.482-2714A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681607 | |||||||
| chr12:69681721 | A | T | 115 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(112): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.482-2828T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681721 | |||||||
| chr12:69681755 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-2862G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681755 | |||||||
| chr12:69681757 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.482-2864G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681757 | |||||||
| chr12:69681846 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(110): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.482-2953G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681846 | |||||||
| chr12:69681851 | C | T | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.482-2958G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681851 | |||||||
| chr12:69681938 | G | A | 115 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(112): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.482-3045C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681938 | |||||||
| chr12:69681949 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-3056A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69681949 | |||||||
| chr12:69682058 | G | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-3165C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682058 | |||||||
| chr12:69682081 | C | CA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(37): Show |
45 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.482-3189dupT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682081 | |||||||
| chr12:69682081 | C | CAA | 8 | a0001c0001t0003g0188 a0001c0001t0003g0190 a0001c0001t0004g0049 others(5): Show |
8 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-3190_482-3189d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682081 | |||||||
| chr12:69682081 | C | CAAA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
112 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.482-3191_482-3189d others(5): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682081 | |||||||
| chr12:69682081 | C | CAAAA | 8 | a0001c0001t0001g0112 a0001c0001t0001g0146 a0001c0001t0001g0149 others(5): Show |
8 | HG00609.hp1 HG00621.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-3192_482-3189d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682081 | |||||||
| chr12:69682081 | C | CAAAAA | 111 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.482-3193_482-3189d others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682081 | |||||||
| chr12:69682153 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-3260A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682153 | |||||||
| chr12:69682255 | C | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
10 | HG01891.hp2 HG02451.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.482-3362G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682255 | |||||||
| chr12:69682386 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-3493A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682386 | |||||||
| chr12:69682387 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-3494C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682387 | |||||||
| chr12:69682486 | G | A | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-3593C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682486 | |||||||
| chr12:69682525 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-3632T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682525 | |||||||
| chr12:69682571 | A | AT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.482-3679_482-3678i others(3): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682571 | |||||||
| chr12:69682571 | A | ATT | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0007c0012t0002g0311 |
3 | HG03831.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-3679_482-3678i others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682571 | |||||||
| chr12:69682572 | A | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-3679T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682572 | |||||||
| chr12:69682596 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.482-3703C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682596 | |||||||
| chr12:69682607 | C | T | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-3714G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682607 | |||||||
| chr12:69682627 | G | T | 1 | a0002c0002t0002g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.482-3734C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682627 | |||||||
| chr12:69682685 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-3792A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682685 | |||||||
| chr12:69682712 | G | A | 15 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.482-3819C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682712 | |||||||
| chr12:69682822 | C | T | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-3929G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682822 | |||||||
| chr12:69682903 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0079 others(2): Show |
7 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-4010A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682903 | |||||||
| chr12:69682906 | ATAAACT | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.482-4019_482-4014d others(8): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682906 | |||||||
| chr12:69682976 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.482-4083A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69682976 | |||||||
| chr12:69683278 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-4385A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683278 | |||||||
| chr12:69683342 | A | T | 4 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4449T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683342 | |||||||
| chr12:69683500 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.482-4607T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683500 | |||||||
| chr12:69683516 | G | A | 1 | a0001c0001t0007g0236 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.482-4623C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683516 | |||||||
| chr12:69683610 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.482-4717G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683610 | |||||||
| chr12:69683623 | AT | A | 3 | a0004c0005t0005g0213 a0004c0005t0005g0214 a0004c0005t0005g0215 |
3 | HG02559.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.482-4731delA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683623 | |||||||
| chr12:69683732 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-4839G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683732 | |||||||
| chr12:69683780 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-4887A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683780 | |||||||
| chr12:69683793 | C | T | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-4900G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683793 | |||||||
| chr12:69683867 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-4974G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683867 | |||||||
| chr12:69683981 | T | C | 3 | a0001c0001t0002g0301 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG01361.hp1 HG02135.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.482-5088A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69683981 | |||||||
| chr12:69684010 | C | T | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-5117G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684010 | |||||||
| chr12:69684023 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-5130C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684023 | |||||||
| chr12:69684050 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.482-5157G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684050 | |||||||
| chr12:69684056 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-5163C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684056 | |||||||
| chr12:69684103 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0132 |
2 | NA18953.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.482-5210G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684103 | |||||||
| chr12:69684172 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0149 a0001c0001t0001g0156 others(1): Show |
6 | NA18945.hp1 NA18955.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-5279C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684172 | |||||||
| chr12:69684203 | G | A | 5 | a0001c0001t0004g0040 a0001c0001t0004g0052 a0001c0001t0004g0053 others(2): Show |
5 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-5310C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684203 | |||||||
| chr12:69684206 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482-5313A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684206 | |||||||
| chr12:69684344 | G | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-5451C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684344 | |||||||
| chr12:69684380 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482-5487A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684380 | |||||||
| chr12:69684392 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.482-5499G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684392 | |||||||
| chr12:69684576 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.482-5683A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684576 | |||||||
| chr12:69684599 | C | T | 1 | a0001c0001t0015g0182 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-5706G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684599 | |||||||
| chr12:69684607 | T | C | 15 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.482-5714A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684607 | |||||||
| chr12:69684617 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.482-5724C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684617 | |||||||
| chr12:69684672 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.482-5779T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684672 | |||||||
| chr12:69684702 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.482-5809G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684702 | |||||||
| chr12:69684795 | T | G | 80 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(77): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.482-5902A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684795 | |||||||
| chr12:69684904 | T | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.482-6011A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684904 | |||||||
| chr12:69684981 | G | GTTCTA | 65 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
72 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.482-6093_482-6089d others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | G | GTTCTATT others(3): Show |
54 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0030 others(51): Show |
61 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.482-6098_482-6089d others(12): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | G | GTTCTATT others(8): Show |
22 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0114 others(19): Show |
24 | HG00099.hp2 HG00733.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.482-6103_482-6089d others(17): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | G | GTTCTATT others(13): Show |
6 | a0001c0001t0001g0205 a0001c0001t0001g0308 a0001c0001t0002g0288 others(3): Show |
6 | HG02818.hp1 HG03688.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-6108_482-6089d others(22): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | GTTCTA | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(34): Show |
47 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.482-6093_482-6089d others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | GTTCTATT others(3): Show |
G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
8 | HG01516.hp2 HG01517.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-6098_482-6089d others(12): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | GTTCTATT others(8): Show |
G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0219 |
2 | HG01934.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.482-6103_482-6089d others(17): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69684981 | GTTCTATT others(13): Show |
G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0218 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.482-6108_482-6089d others(22): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69684981 | |||||||
| chr12:69685029 | C | CTATTCTA others(6): Show |
1 | a0001c0001t0003g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.482-6137_482-6136i others(15): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685029 | |||||||
| chr12:69685029 | C | CTATTCTA others(11): Show |
1 | a0001c0001t0003g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.482-6137_482-6136i others(20): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685029 | |||||||
| chr12:69685029 | C | CTATTCTA others(21): Show |
2 | a0001c0001t0003g0055 a0001c0001t0003g0194 |
2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.482-6137_482-6136i others(30): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685029 | |||||||
| chr12:69685029 | C | CTATTCTA others(26): Show |
1 | a0001c0001t0003g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482-6137_482-6136i others(35): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685029 | |||||||
| chr12:69685185 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.482-6292A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685185 | |||||||
| chr12:69685273 | T | A | 1 | a0001c0001t0002g0289 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.482-6380A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685273 | |||||||
| chr12:69685389 | A | G | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-6496T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685389 | |||||||
| chr12:69685410 | G | A | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.482-6517C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685410 | |||||||
| chr12:69685483 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0162 |
2 | NA18965.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.482-6590A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685483 | |||||||
| chr12:69685554 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0005g0203 a0001c0006t0006g0204 |
3 | NA18906.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.482-6661C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685554 | |||||||
| chr12:69685607 | T | C | 80 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(77): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.482-6714A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685607 | |||||||
| chr12:69685773 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.482-6880G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685773 | |||||||
| chr12:69685859 | G | C | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.482-6966C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69685859 | |||||||
| chr12:69686002 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
137 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.482-7109C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686002 | |||||||
| chr12:69686010 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.482-7117G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686010 | |||||||
| chr12:69686185 | G | GA | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
96 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.482-7293dupT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686185 | |||||||
| chr12:69686185 | G | GAAA | 14 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(11): Show |
15 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.482-7295_482-7293d others(5): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686185 | |||||||
| chr12:69686185 | G | GAAAAA | 10 | a0001c0001t0003g0031 a0001c0001t0003g0185 a0001c0001t0003g0186 others(7): Show |
11 | HG01081.hp1 HG01109.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-7297_482-7293d others(7): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686185 | |||||||
| chr12:69686199 | C | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.482-7306G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686199 | |||||||
| chr12:69686344 | G | A | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481+7330C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686344 | |||||||
| chr12:69686373 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
106 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.481+7301T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686373 | |||||||
| chr12:69686411 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.481+7263C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686411 | |||||||
| chr12:69686556 | G | A | 4 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+7118C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686556 | |||||||
| chr12:69686601 | G | A | 7 | a0001c0001t0007g0236 a0001c0006t0006g0184 a0001c0006t0006g0237 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+7073C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686601 | |||||||
| chr12:69686771 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0113 a0001c0001t0001g0308 a0001c0001t0002g0264 others(3): Show |
6 | HG01070.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+6888_481+6902d others(17): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686771 | |||||||
| chr12:69686771 | C | CAAAAAAA others(9): Show |
66 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(63): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.481+6887_481+6902d others(18): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686771 | |||||||
| chr12:69686771 | C | CAAAAAAA others(10): Show |
12 | a0001c0001t0002g0065 a0001c0001t0002g0259 a0001c0001t0002g0291 others(9): Show |
12 | HG00438.hp2 HG02723.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+6886_481+6902d others(19): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686771 | |||||||
| chr12:69686771 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.481+6902_481+6903i others(18): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686771 | |||||||
| chr12:69686779 | C | CA | 12 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0123 others(9): Show |
14 | HG02083.hp2 NA18948.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+6894dupT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686779 | |||||||
| chr12:69686779 | C | CAAAAAAA others(9): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0097 others(19): Show |
26 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.481+6894_481+6895i others(18): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686779 | |||||||
| chr12:69686779 | C | CAAAAAAA others(8): Show |
67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
83 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.481+6894_481+6895i others(17): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686779 | |||||||
| chr12:69686779 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.481+6894_481+6895i others(16): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686779 | |||||||
| chr12:69686779 | C | CGAAAAAA others(8): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.481+6894_481+6895i others(17): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686779 | |||||||
| chr12:69686786 | A | AAAAAAAA others(7): Show |
5 | a0001c0001t0002g0195 a0001c0001t0003g0191 a0001c0001t0003g0192 others(2): Show |
5 | HG01081.hp1 HG03195.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+6887_481+6888i others(16): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | AAAAAAAA others(6): Show |
8 | a0001c0001t0003g0031 a0001c0001t0003g0055 a0001c0001t0003g0185 others(5): Show |
9 | HG01109.hp2 HG02258.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+6887_481+6888i others(15): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | AAAAAAAA others(5): Show |
14 | a0001c0001t0004g0040 a0001c0001t0004g0044 a0001c0001t0004g0046 others(11): Show |
15 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.481+6887_481+6888i others(14): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | AAAAAAAA others(4): Show |
3 | a0001c0001t0004g0042 a0001c0006t0006g0184 a0001c0006t0006g0237 |
3 | HG01256.hp1 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.481+6887_481+6888i others(13): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | AAAAAAAA others(3): Show |
6 | a0001c0001t0007g0236 a0004c0005t0005g0206 a0004c0005t0005g0213 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+6887_481+6888i others(12): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | AAAAAAAA others(1): Show |
34 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(31): Show |
36 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.481+6887_481+6888i others(10): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686786 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.481+6888T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686786 | |||||||
| chr12:69686807 | G | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0064 others(12): Show |
18 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+6867C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686807 | |||||||
| chr12:69686892 | G | T | 2 | a0001c0004t0011g0060 a0001c0004t0011g0061 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.481+6782C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686892 | |||||||
| chr12:69686972 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.481+6702A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69686972 | |||||||
| chr12:69687259 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481+6415T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687259 | |||||||
| chr12:69687472 | AGAAAAAA others(2): Show |
A | 72 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(69): Show |
78 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.481+6193_481+6201d others(11): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687472 | |||||||
| chr12:69687529 | C | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(40): Show |
47 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.481+6145G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687529 | |||||||
| chr12:69687532 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.481+6142G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687532 | |||||||
| chr12:69687640 | G | A | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+6034C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687640 | |||||||
| chr12:69687663 | C | CA | 87 | a0001c0001t0001g0175 a0001c0001t0001g0272 a0001c0001t0001g0274 others(84): Show |
95 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.481+6010dupT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687663 | |||||||
| chr12:69687663 | C | CAA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.481+6009_481+6010d others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687663 | |||||||
| chr12:69687663 | C | CAAA | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
66 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.481+6008_481+6010d others(5): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687663 | |||||||
| chr12:69687663 | CA | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(49): Show |
57 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.481+6010delT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687663 | |||||||
| chr12:69687775 | CTATT | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02135.hp2 NA18979.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+5895_481+5898d others(6): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687775 | |||||||
| chr12:69687817 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.481+5857T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687817 | |||||||
| chr12:69687841 | C | T | 29 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(26): Show |
31 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.481+5833G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69687841 | |||||||
| chr12:69688082 | T | C | 2 | a0001c0001t0010g0239 a0001c0006t0006g0238 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.481+5592A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688082 | |||||||
| chr12:69688277 | G | T | 2 | a0001c0004t0011g0060 a0001c0004t0011g0061 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.481+5397C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688277 | |||||||
| chr12:69688364 | A | T | 4 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+5310T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688364 | |||||||
| chr12:69688547 | G | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(9): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.481+5127C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688547 | |||||||
| chr12:69688577 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.481+5097C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688577 | |||||||
| chr12:69688629 | A | G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(69): Show |
78 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.481+5045T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688629 | |||||||
| chr12:69688665 | C | A | 1 | a0001c0001t0003g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.481+5009G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688665 | |||||||
| chr12:69688756 | C | A | 13 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(10): Show |
14 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+4918G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688756 | |||||||
| chr12:69688760 | T | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(40): Show |
47 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.481+4914A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688760 | |||||||
| chr12:69688978 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
11 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.481+4696C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688978 | |||||||
| chr12:69688986 | A | G | 4 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+4688T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69688986 | |||||||
| chr12:69689123 | A | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.481+4551T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689123 | |||||||
| chr12:69689302 | T | C | 5 | a0001c0001t0003g0055 a0001c0001t0003g0191 a0001c0001t0003g0192 others(2): Show |
5 | HG01081.hp1 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+4372A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689302 | |||||||
| chr12:69689332 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.481+4342G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689332 | |||||||
| chr12:69689362 | C | T | 3 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 |
3 | HG01081.hp2 HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.481+4312G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689362 | |||||||
| chr12:69689434 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.481+4240C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689434 | |||||||
| chr12:69689434 | G | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(69): Show |
78 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.481+4240C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689434 | |||||||
| chr12:69689984 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0172 a0001c0001t0001g0173 |
4 | NA18969.hp2 NA19060.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+3690A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69689984 | |||||||
| chr12:69690263 | A | T | 1 | a0001c0001t0002g0256 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.481+3411T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690263 | |||||||
| chr12:69690269 | A | G | 63 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(60): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.481+3405T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690269 | |||||||
| chr12:69690356 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.481+3318A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690356 | |||||||
| chr12:69690372 | G | C | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+3302C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690372 | |||||||
| chr12:69690398 | A | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.481+3276T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690398 | |||||||
| chr12:69690453 | T | C | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.481+3221A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690453 | |||||||
| chr12:69690650 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.481+3024C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690650 | |||||||
| chr12:69690797 | G | C | 24 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0216 others(21): Show |
26 | HG01167.hp1 HG01243.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.481+2877C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690797 | |||||||
| chr12:69690871 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.481+2803T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690871 | |||||||
| chr12:69690952 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.481+2722G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69690952 | |||||||
| chr12:69691015 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.481+2659C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691015 | |||||||
| chr12:69691254 | A | G | 1 | a0002c0002t0002g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.481+2420T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691254 | |||||||
| chr12:69691291 | T | C | 2 | a0001c0001t0002g0298 a0001c0001t0014g0297 |
2 | HG00423.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.481+2383A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691291 | |||||||
| chr12:69691561 | G | A | 14 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.481+2113C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691561 | |||||||
| chr12:69691603 | C | T | 1 | a0001c0006t0006g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.481+2071G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691603 | |||||||
| chr12:69691664 | C | T | 86 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(83): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.481+2010G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691664 | |||||||
| chr12:69691665 | G | C | 86 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(83): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.481+2009C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691665 | |||||||
| chr12:69691684 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.481+1990G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691684 | |||||||
| chr12:69691685 | G | T | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481+1989C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691685 | |||||||
| chr12:69691707 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.481+1967C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691707 | |||||||
| chr12:69691771 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.481+1903T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691771 | |||||||
| chr12:69691807 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.481+1867C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691807 | |||||||
| chr12:69691850 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(10): Show |
15 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+1824A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69691850 | |||||||
| chr12:69692677 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(10): Show |
15 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+997C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69692677 | |||||||
| chr12:69692894 | C | T | 1 | a0001c0001t0001g0011 | 3 | HG02451.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.481+780G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69692894 | |||||||
| chr12:69693059 | A | G | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481+615T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693059 | |||||||
| chr12:69693110 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.481+564G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693110 | |||||||
| chr12:69693159 | T | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.481+515A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693159 | |||||||
| chr12:69693231 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.481+443A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693231 | |||||||
| chr12:69693245 | C | CT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
166 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.481+428dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693245 | |||||||
| chr12:69693245 | C | CTT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0064 others(12): Show |
18 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+427_481+428dup others(2): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693245 | |||||||
| chr12:69693263 | C | CT | 14 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+410dupA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693263 | |||||||
| chr12:69693263 | CT | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.481+410delA | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693263 | |||||||
| chr12:69693263 | CTT | C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(36): Show |
43 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.481+409_481+410del others(2): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693263 | |||||||
| chr12:69693284 | G | T | 4 | a0001c0001t0002g0110 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+390C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693284 | |||||||
| chr12:69693349 | C | T | 1 | a0001c0006t0006g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.481+325G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693349 | |||||||
| chr12:69693350 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+324C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693350 | |||||||
| chr12:69693520 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | NA18747.hp1 NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.481+154G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693520 | |||||||
| chr12:69693527 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481+147T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693527 | |||||||
| chr12:69693588 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.481+86T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 4/9 | chr12 | 69693588 | |||||||
| chr12:69694043 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.248-136G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 3/9 | chr12 | 69694043 | |||||||
| chr12:69694291 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.247+79T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 3/9 | chr12 | 69694291 | |||||||
| chr12:69694305 | AGT | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
100 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.247+63_247+64delAC | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 3/9 | chr12 | 69694305 | |||||||
| chr12:69694352 | C | T | 59 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(56): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.247+18G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 3/9 | chr12 | 69694352 | |||||||
| chr12:69694477 | T | A | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-13A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694477 | |||||||
| chr12:69694564 | T | C | 8 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG00280.hp1 HG01361.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-100A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694564 | |||||||
| chr12:69694567 | T | G | 1 | a0001c0001t0007g0236 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-103A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694567 | |||||||
| chr12:69694604 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.153-140T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694604 | |||||||
| chr12:69694616 | CA | C | 23 | a0001c0001t0001g0032 a0001c0001t0001g0216 a0001c0001t0001g0217 others(20): Show |
25 | HG01167.hp1 HG01243.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.153-153delT | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694616 | |||||||
| chr12:69694740 | T | C | 1 | a0001c0006t0006g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.153-276A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694740 | |||||||
| chr12:69694861 | G | A | 1 | a0002c0002t0002g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.153-397C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69694861 | |||||||
| chr12:69695190 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.153-726C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695190 | |||||||
| chr12:69695216 | C | T | 4 | a0004c0005t0005g0206 a0004c0005t0005g0213 a0004c0005t0005g0214 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-752G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695216 | |||||||
| chr12:69695285 | G | A | 15 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-821C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695285 | |||||||
| chr12:69695324 | A | G | 14 | a0001c0001t0002g0195 a0001c0001t0003g0031 a0001c0001t0003g0055 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.153-860T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695324 | |||||||
| chr12:69695436 | A | C | 1 | a0001c0001t0004g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.153-972T>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695436 | |||||||
| chr12:69695476 | C | A | 1 | a0001c0001t0015g0182 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.153-1012G>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695476 | |||||||
| chr12:69695613 | A | G | 1 | a0008c0009t0001g0108 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.153-1149T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695613 | |||||||
| chr12:69695633 | T | C | 1 | a0005c0013t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.153-1169A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695633 | |||||||
| chr12:69695649 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG00408.hp1 HG01358.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-1185G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695649 | |||||||
| chr12:69695963 | T | A | 1 | a0001c0006t0006g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.153-1499A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695963 | |||||||
| chr12:69695988 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0199 others(12): Show |
17 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-1524T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69695988 | |||||||
| chr12:69696127 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+1520G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696127 | |||||||
| chr12:69696357 | C | G | 15 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+1290G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696357 | |||||||
| chr12:69696512 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152+1135A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696512 | |||||||
| chr12:69696549 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
116 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.152+1098C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696549 | |||||||
| chr12:69696573 | C | G | 1 | a0004c0005t0005g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.152+1074G>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696573 | |||||||
| chr12:69696591 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.152+1056C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696591 | |||||||
| chr12:69696683 | A | T | 79 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.152+964T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696683 | |||||||
| chr12:69696715 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.152+932A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696715 | |||||||
| chr12:69696800 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152+847T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69696800 | |||||||
| chr12:69697228 | T | G | 2 | a0002c0002t0002g0253 a0002c0002t0002g0254 |
2 | HG01358.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.152+419A>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697228 | |||||||
| chr12:69697404 | G | C | 15 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0044 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+243C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697404 | |||||||
| chr12:69697448 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152+199C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697448 | |||||||
| chr12:69697518 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.152+129T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697518 | |||||||
| chr12:69697576 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.152+71C>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697576 | |||||||
| chr12:69697604 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.152+43G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 2/9 | chr12 | 69697604 | |||||||
| chr12:69697901 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15-88T>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69697901 | |||||||
| chr12:69697920 | A | G | 2 | a0001c0001t0010g0239 a0001c0006t0006g0238 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-15-107T>C | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69697920 | |||||||
| chr12:69697997 | G | A | 1 | a0001c0001t0002g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15-184C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69697997 | |||||||
| chr12:69698081 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0199 others(6): Show |
11 | HG01891.hp2 HG02451.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-268G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698081 | |||||||
| chr12:69698093 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-15-280A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698093 | |||||||
| chr12:69698163 | G | C | 2 | a0001c0001t0002g0310 a0007c0012t0002g0311 |
2 | HG01258.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-15-350C>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698163 | |||||||
| chr12:69698220 | T | C | 59 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0198 others(56): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-15-407A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698220 | |||||||
| chr12:69698270 | T | C | 1 | a0003c0003t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15-457A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698270 | |||||||
| chr12:69698397 | T | C | 1 | a0001c0001t0004g0054 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-15-584A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698397 | |||||||
| chr12:69698430 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-15-617A>G | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698430 | |||||||
| chr12:69698489 | AACAG | A | 82 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0282 others(79): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-680_-15-677del others(4): Show |
BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698489 | |||||||
| chr12:69698495 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-15-682G>A | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698495 | |||||||
| chr12:69698611 | T | A | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-16+594A>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698611 | |||||||
| chr12:69698856 | G | A | 1 | a0001c0001t0010g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-16+349C>T | BEST3 | ENSG00000127325.19 | transcript | ENST00000330891.10 | protein_coding | 1/9 | chr12 | 69698856 |