Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54928 |
| ensemblid | ENSG00000104331.9 |
| hgncid | 26019 |
| symbol | BPNT2 |
| name | 3'(2'), 5'-bisphosphate nucleotidase 2 |
| refseq_nuc | NM_017813.5 |
| refseq_prot | NP_060283.3 |
| ensembl_nuc | ENST00000262644.9 |
| ensembl_prot | ENSP00000262644.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 56957931 |
| end | 56993867 |
| strand | - |
| ver | v1.2 |
| region | chr8:56957931-56993867 |
| region5000 | chr8:56952931-56998867 |
| regionname0 | BPNT2_chr8_56957931_56993867 |
| regionname5000 | BPNT2_chr8_56952931_56998867 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 352 | 75 | 55 | 172 | 10 | 38 | 134 | BPNT2_chr8_56952931_56998867 | BPNT2 | MAPMG others(354): Show |
chr8 | 56952931 | 56998867 |
| a0002 | 0/0 | 359 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | MAPMG others(354): Show |
chr8 | 56952931 | 56998867 |
| a0003 | 0/0 | 359 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | MAPMG others(354): Show |
chr8 | 56952931 | 56998867 |
| a0004 | 0/0 | 359 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | MAPMG others(354): Show |
chr8 | 56952931 | 56998867 |
| a0005 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | MAPMG others(354): Show |
chr8 | 56952931 | 56998867 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 349 | 72 | 55 | 172 | 10 | 38 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 | ||
| a0001c0002 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 | ||
| a0002c0005 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 | ||
| a0003c0006 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 | ||
| a0004c0003 | 0/0 | 1077 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 | ||
| a0005c0004 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ATGGC others(1072): Show |
chr8 | 56952931 | 56998867 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7224 | 142 | 36 | 24 | 59 | 8 | 14 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0002 | 0/0 | 7224 | 53 | 6 | 9 | 32 | 0 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0003 | 0/0 | 7224 | 52 | 0 | 2 | 44 | 0 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0004 | 1/0 | 7224 | 41 | 7 | 4 | 22 | 0 | 7 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0005 | 0/0 | 7224 | 6 | 0 | 6 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0006 | 0/0 | 7217 | 5 | 4 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7212): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0007 | 0/0 | 7224 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0008 | 0/0 | 7223 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7218): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0009 | 0/0 | 7224 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0010 | 0/0 | 7224 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0011 | 0/0 | 7224 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0012 | 0/0 | 7224 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0013 | 0/0 | 7224 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0014 | 0/0 | 7220 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7215): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0015 | 0/0 | 7224 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0016 | 0/0 | 7224 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0017 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0018 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0019 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0020 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0021 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0022 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0023 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0026 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0027 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7218): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0028 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7218): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0029 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0030 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0031 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0032 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0033 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7218): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0034 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0035 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0001t0036 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0002t0024 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0002t0025 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0001c0002t0037 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0002c0005t0002 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0003c0006t0003 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0004c0003t0001 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| a0005c0004t0013 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | ACCTC others(7219): Show |
chr8 | 56952931 | 56998867 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 12 | 0 | 1 | 9 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0008 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0002 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0004 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0005g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0005g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0008g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0011g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0012g0011 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0014g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0015g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0015g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0016g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0017g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0018g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0021g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0022g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0023g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0026g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0027g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0028g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0029g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0030g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0031g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0032g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0033g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0034g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0035g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0001t0036g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0002t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0002t0025g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0001c0002t0037g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0002c0005t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0003c0006t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0004c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| a0005c0004t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00323 | hp1 | a0002 | c0005 | t0002 | g0198 | EUR | FIN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00621 | hp2 | a0001 | c0001 | t0017 | g0119 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00738 | hp1 | a0001 | c0001 | t0018 | g0129 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0184 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01070 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01071 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01099 | hp2 | a0001 | c0001 | t0022 | g0079 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01175 | hp1 | a0001 | c0001 | t0029 | g0178 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01358 | hp1 | a0001 | c0001 | t0036 | g0254 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01516 | hp2 | a0003 | c0006 | t0003 | g0248 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01952 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02055 | hp2 | a0001 | c0002 | t0024 | g0181 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0189 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0253 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0197 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02293 | hp2 | a0004 | c0003 | t0001 | g0044 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02300 | hp2 | a0001 | c0001 | t0011 | g0108 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02451 | hp1 | a0001 | c0002 | t0037 | g0256 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0088 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0208 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02717 | hp2 | a0001 | c0001 | t0033 | g0046 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02723 | hp2 | a0005 | c0004 | t0013 | g0188 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02886 | hp1 | a0001 | c0001 | t0030 | g0187 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02922 | hp2 | a0001 | c0001 | t0032 | g0089 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0177 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0092 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03041 | hp2 | a0001 | c0001 | t0028 | g0047 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0202 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03486 | hp2 | a0001 | c0002 | t0025 | g0182 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0137 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0011 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03704 | hp1 | a0001 | c0001 | t0012 | g0011 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0077 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03942 | hp1 | a0001 | c0001 | t0035 | g0196 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0123 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18942 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18971 | hp2 | a0001 | c0001 | t0015 | g0134 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18980 | hp1 | a0001 | c0001 | t0008 | g0071 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18990 | hp1 | a0001 | c0001 | t0015 | g0138 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19055 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19083 | hp2 | a0001 | c0001 | t0034 | g0194 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19088 | hp1 | a0001 | c0001 | t0026 | g0122 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ASW | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ASW | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20752 | hp2 | a0001 | c0001 | t0012 | g0011 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20805 | hp2 | a0001 | c0001 | t0020 | g0126 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20905 | hp2 | a0001 | c0001 | t0031 | g0145 | SAS | GIH | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02109 | hp1 | a0001 | c0001 | t0027 | g0045 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | USA | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0069 | REF | REF | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:56963909 | C | T | 1 | a0002 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.964G>A | p.Glu322Lys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1246/7224 | 964/1080 | 322/359 | chr8 | 56963909 | |||
| chr8:56964017 | T | C | 1 | a0003 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.856A>G | p.Lys286Glu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1138/7224 | 856/1080 | 286/359 | chr8 | 56964017 | |||
| chr8:56993326 | C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.260G>C | p.Ser87Thr | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 542/7224 | 260/1080 | 87/359 | chr8 | 56993326 | |||
| chr8:56993329 | T | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.257A>G | p.Glu86Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 539/7224 | 257/1080 | 86/359 | chr8 | 56993329 | |||
| chr8:56993330 | C | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.256G>A | p.Glu86Lys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 538/7224 | 256/1080 | 86/359 | chr8 | 56993330 | |||
| chr8:56993338 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.248G>T | p.Arg83Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 530/7224 | 248/1080 | 83/359 | chr8 | 56993338 | |||
| chr8:56993341 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.245G>T | p.Arg82Met | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 527/7224 | 245/1080 | 82/359 | chr8 | 56993341 | |||
| chr8:56993342 | T | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.244A>T | p.Arg82Trp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 526/7224 | 244/1080 | 82/359 | chr8 | 56993342 | |||
| chr8:56993344 | A | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.242T>A | p.Val81Glu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 524/7224 | 242/1080 | 81/359 | chr8 | 56993344 | |||
| chr8:56993347 | T | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.239A>T | p.Glu80Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 521/7224 | 239/1080 | 80/359 | chr8 | 56993347 | |||
| chr8:56993348 | C | A | 1 | a0005 | 1 | HG02723.hp2 | stop_gained | HIGH | c.238G>T | p.Glu80* | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 520/7224 | 238/1080 | 80/359 | chr8 | 56993348 | |||
| chr8:56993350 | T | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.236A>C | p.Asp79Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 518/7224 | 236/1080 | 79/359 | chr8 | 56993350 | |||
| chr8:56993351 | C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.235G>C | p.Asp79His | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 517/7224 | 235/1080 | 79/359 | chr8 | 56993351 | |||
| chr8:56993353 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.233G>T | p.Gly78Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 515/7224 | 233/1080 | 78/359 | chr8 | 56993353 | |||
| chr8:56993354 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.232G>T | p.Gly78Cys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 514/7224 | 232/1080 | 78/359 | chr8 | 56993354 | |||
| chr8:56993356 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.230G>T | p.Gly77Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 512/7224 | 230/1080 | 77/359 | chr8 | 56993356 | |||
| chr8:56993363 | C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.223G>C | p.Val75Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 505/7224 | 223/1080 | 75/359 | chr8 | 56993363 | |||
| chr8:56993366 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.220G>T | p.Ala74Ser | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 502/7224 | 220/1080 | 74/359 | chr8 | 56993366 | |||
| chr8:56993368 | G | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.218C>G | p.Ala73Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 500/7224 | 218/1080 | 73/359 | chr8 | 56993368 | |||
| chr8:56993388 | C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.198G>C | p.Met66Ile | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 480/7224 | 198/1080 | 66/359 | chr8 | 56993388 | |||
| chr8:56993389 | A | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.197T>G | p.Met66Arg | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 479/7224 | 197/1080 | 66/359 | chr8 | 56993389 | |||
| chr8:56993390 | T | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.196A>C | p.Met66Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 478/7224 | 196/1080 | 66/359 | chr8 | 56993390 | |||
| chr8:56993391 | C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.195G>T | p.Glu65Asp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 477/7224 | 195/1080 | 65/359 | chr8 | 56993391 | |||
| chr8:56993396 | G | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.190C>A | p.Arg64Ser | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 472/7224 | 190/1080 | 64/359 | chr8 | 56993396 | |||
| chr8:56993397 | C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.189G>C | p.Leu63Phe | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 471/7224 | 189/1080 | 63/359 | chr8 | 56993397 | |||
| chr8:56993398 | A | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.188T>G | p.Leu63Trp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 470/7224 | 188/1080 | 63/359 | chr8 | 56993398 | |||
| chr8:56993399 | A | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.187T>A | p.Leu63Met | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 469/7224 | 187/1080 | 63/359 | chr8 | 56993399 | |||
| chr8:56993413 | C | G | 1 | a0004 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.173G>C | p.Gly58Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 455/7224 | 173/1080 | 58/359 | chr8 | 56993413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:56963934 | C | T | 1 | a0001c0002 | 3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.939G>A | p.Gly313Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1221/7224 | 939/1080 | 313/359 | chr8 | 56963934 | |||
| chr8:56993331 | G | C | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.255C>G | p.Arg85Arg | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 537/7224 | 255/1080 | 85/359 | chr8 | 56993331 | |||
| chr8:56993343 | C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.243G>C | p.Val81Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 525/7224 | 243/1080 | 81/359 | chr8 | 56993343 | |||
| chr8:56993364 | T | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.222A>C | p.Ala74Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 504/7224 | 222/1080 | 74/359 | chr8 | 56993364 | |||
| chr8:56993370 | C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.216G>C | p.Leu72Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 498/7224 | 216/1080 | 72/359 | chr8 | 56993370 | |||
| chr8:56993373 | C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.213G>C | p.Val71Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 495/7224 | 213/1080 | 71/359 | chr8 | 56993373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:56958063 | T | C | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0036 |
12 | HG01074.hp1 HG01168.hp1 HG01358.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5730A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5730 | chr8 | 56958063 | ||||||
| chr8:56958159 | T | C | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5634A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5634 | chr8 | 56958159 | ||||||
| chr8:56958281 | A | G | 3 | a0001c0001t0006 a0001c0001t0027 a0001c0001t0033 |
7 | HG00741.hp1 HG02109.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5512T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5512 | chr8 | 56958281 | ||||||
| chr8:56958288 | T | C | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
306 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*5505A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5505 | chr8 | 56958288 | ||||||
| chr8:56958301 | C | T | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5492G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5492 | chr8 | 56958301 | ||||||
| chr8:56958491 | G | A | 2 | a0001c0001t0028 a0001c0002t0024 |
2 | HG02055.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5302C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5302 | chr8 | 56958491 | ||||||
| chr8:56958659 | T | C | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5134A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5134 | chr8 | 56958659 | ||||||
| chr8:56958779 | T | C | 8 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0027 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5014A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5014 | chr8 | 56958779 | ||||||
| chr8:56958903 | G | A | 6 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0016 others(3): Show |
60 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4890C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4890 | chr8 | 56958903 | ||||||
| chr8:56959134 | A | G | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4659T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4659 | chr8 | 56959134 | ||||||
| chr8:56959363 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4430A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4430 | chr8 | 56959363 | ||||||
| chr8:56959478 | G | A | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4315C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4315 | chr8 | 56959478 | ||||||
| chr8:56959529 | C | T | 1 | a0001c0001t0020 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4264G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4264 | chr8 | 56959529 | ||||||
| chr8:56959584 | C | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4209G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4209 | chr8 | 56959584 | ||||||
| chr8:56959667 | AGAT | A | 1 | a0001c0001t0006 | 5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4123_*4125delATC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4123 | chr8 | 56959667 | ||||||
| chr8:56959836 | G | T | 1 | a0001c0002t0024 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3957C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3957 | chr8 | 56959836 | ||||||
| chr8:56959882 | C | T | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3911G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3911 | chr8 | 56959882 | ||||||
| chr8:56960062 | A | C | 1 | a0001c0001t0015 | 2 | NA18971.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3731 | chr8 | 56960062 | ||||||
| chr8:56960120 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*3673A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3673 | chr8 | 56960120 | ||||||
| chr8:56960492 | T | A | 1 | a0001c0001t0022 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3301A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3301 | chr8 | 56960492 | ||||||
| chr8:56960589 | T | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0029 others(2): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3204A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3204 | chr8 | 56960589 | ||||||
| chr8:56960715 | A | C | 1 | a0001c0001t0032 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3078T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3078 | chr8 | 56960715 | ||||||
| chr8:56960715 | AT | A | 1 | a0001c0001t0008 | 5 | NA18939.hp2 NA18965.hp1 NA18980.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3077delA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3077 | chr8 | 56960715 | ||||||
| chr8:56960848 | T | C | 1 | a0001c0001t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2945A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2945 | chr8 | 56960848 | ||||||
| chr8:56960930 | A | G | 1 | a0001c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2863T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2863 | chr8 | 56960930 | ||||||
| chr8:56961162 | T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2631A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2631 | chr8 | 56961162 | ||||||
| chr8:56961185 | T | G | 1 | a0001c0001t0012 | 3 | HG03669.hp2 HG03704.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2608A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2608 | chr8 | 56961185 | ||||||
| chr8:56961285 | A | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2508T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2508 | chr8 | 56961285 | ||||||
| chr8:56961411 | T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2382A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2382 | chr8 | 56961411 | ||||||
| chr8:56961505 | C | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2288G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2288 | chr8 | 56961505 | ||||||
| chr8:56961644 | C | A | 3 | a0001c0002t0024 a0001c0002t0025 a0001c0002t0037 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2149G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2149 | chr8 | 56961644 | ||||||
| chr8:56961796 | C | T | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1997 | chr8 | 56961796 | ||||||
| chr8:56961840 | C | T | 1 | a0001c0001t0035 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1953 | chr8 | 56961840 | ||||||
| chr8:56962142 | C | T | 1 | a0001c0001t0018 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1651G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1651 | chr8 | 56962142 | ||||||
| chr8:56962195 | G | A | 1 | a0001c0001t0026 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1598C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1598 | chr8 | 56962195 | ||||||
| chr8:56962300 | A | G | 1 | a0001c0001t0036 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1493 | chr8 | 56962300 | ||||||
| chr8:56962479 | CG | C | 3 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0033 |
3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1313delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1313 | chr8 | 56962479 | ||||||
| chr8:56962812 | TA | T | 2 | a0001c0001t0006 a0001c0001t0014 |
7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*980delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 980 | chr8 | 56962812 | ||||||
| chr8:56962926 | A | G | 1 | a0001c0001t0017 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 867 | chr8 | 56962926 | ||||||
| chr8:56963011 | C | T | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0029 others(2): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 782 | chr8 | 56963011 | ||||||
| chr8:56963029 | G | A | 4 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0035 others(1): Show |
57 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 764 | chr8 | 56963029 | ||||||
| chr8:56963092 | G | A | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0029 others(3): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*701C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 701 | chr8 | 56963092 | ||||||
| chr8:56963240 | T | C | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 553 | chr8 | 56963240 | ||||||
| chr8:56963286 | TACA | T | 2 | a0001c0001t0006 a0001c0001t0014 |
7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*506delTGT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 504 | chr8 | 56963286 | ||||||
| chr8:56963435 | C | T | 1 | a0001c0001t0011 | 3 | HG01081.hp2 HG01952.hp2 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*358G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 358 | chr8 | 56963435 | ||||||
| chr8:56963646 | G | A | 2 | a0001c0001t0010 a0001c0001t0032 |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 147 | chr8 | 56963646 | ||||||
| chr8:56963708 | T | C | 1 | a0001c0001t0033 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 85 | chr8 | 56963708 | ||||||
| chr8:56993710 | G | A | 7 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0016 others(4): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | chr8 | 56993710 | |||||||
| chr8:56993754 | G | A | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0036 others(1): Show |
60 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-169C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 169 | chr8 | 56993754 | ||||||
| chr8:56993848 | T | C | 1 | a0001c0002t0037 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-263A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 263 | chr8 | 56993848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:56964123 | C | G | 1 | a0001c0001t0003g0246 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.809-59G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964123 | |||||||
| chr8:56964163 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0222 |
2 | HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.809-99A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964163 | |||||||
| chr8:56964340 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-276A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964340 | |||||||
| chr8:56964359 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.809-295G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964359 | |||||||
| chr8:56964414 | C | T | 3 | a0001c0001t0027g0045 a0001c0001t0028g0047 a0001c0001t0033g0046 |
3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.809-350G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964414 | |||||||
| chr8:56964448 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.809-384C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964448 | |||||||
| chr8:56964469 | T | TTTTTGTA | 5 | a0001c0001t0001g0094 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02040.hp1 HG02080.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-412_809-406dup others(7): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964469 | |||||||
| chr8:56964483 | A | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0001t0001g0155 others(3): Show |
7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-419T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964483 | |||||||
| chr8:56964527 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0166 a0001c0001t0001g0176 |
4 | HG01109.hp2 HG02055.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-463A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964527 | |||||||
| chr8:56964551 | T | C | 1 | a0001c0001t0004g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.809-487A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964551 | |||||||
| chr8:56964567 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.809-503G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964567 | |||||||
| chr8:56964581 | G | A | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.809-517C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964581 | |||||||
| chr8:56964675 | T | C | 1 | a0001c0001t0033g0046 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-611A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964675 | |||||||
| chr8:56964703 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.809-639A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964703 | |||||||
| chr8:56964710 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809-646G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964710 | |||||||
| chr8:56964774 | C | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-710G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964774 | |||||||
| chr8:56964775 | G | A | 1 | a0001c0001t0004g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.809-711C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964775 | |||||||
| chr8:56965058 | G | A | 36 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(33): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.809-994C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965058 | |||||||
| chr8:56965115 | C | T | 1 | a0001c0001t0022g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.809-1051G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965115 | |||||||
| chr8:56965136 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0240 |
3 | HG02135.hp2 HG02523.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.808+1055C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965136 | |||||||
| chr8:56965260 | G | A | 3 | a0001c0001t0003g0233 a0001c0001t0003g0234 a0001c0001t0003g0237 |
3 | NA18941.hp2 NA18947.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.808+931C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965260 | |||||||
| chr8:56965275 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+916G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965275 | |||||||
| chr8:56965514 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.808+677A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965514 | |||||||
| chr8:56965557 | T | C | 1 | a0001c0001t0004g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.808+634A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965557 | |||||||
| chr8:56965697 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.808+494G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965697 | |||||||
| chr8:56965755 | T | C | 47 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.808+436A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965755 | |||||||
| chr8:56965818 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.808+373G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965818 | |||||||
| chr8:56965878 | C | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.808+313G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965878 | |||||||
| chr8:56966040 | G | T | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.808+151C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56966040 | |||||||
| chr8:56966148 | G | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0116 a0001c0001t0001g0147 others(2): Show |
6 | NA18948.hp1 NA18977.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+43C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56966148 | |||||||
| chr8:56966431 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-79A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966431 | |||||||
| chr8:56966724 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.647-372G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966724 | |||||||
| chr8:56966879 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.647-527A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966879 | |||||||
| chr8:56966999 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.647-647A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966999 | |||||||
| chr8:56967096 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-744C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967096 | |||||||
| chr8:56967262 | T | C | 1 | a0001c0001t0030g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.647-910A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967262 | |||||||
| chr8:56967418 | A | G | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-1066T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967418 | |||||||
| chr8:56967456 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.647-1104G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967456 | |||||||
| chr8:56967634 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647-1282G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967634 | |||||||
| chr8:56967784 | G | T | 2 | a0001c0001t0001g0146 a0001c0001t0031g0145 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.647-1432C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967784 | |||||||
| chr8:56967895 | C | T | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.647-1543G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967895 | |||||||
| chr8:56968210 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.647-1858A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968210 | |||||||
| chr8:56968300 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.647-1948A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968300 | |||||||
| chr8:56968305 | A | C | 1 | a0001c0001t0006g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.647-1953T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968305 | |||||||
| chr8:56968306 | A | G | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-1954T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968306 | |||||||
| chr8:56968344 | G | A | 1 | a0001c0001t0026g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.647-1992C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968344 | |||||||
| chr8:56968389 | T | TA | 42 | a0001c0001t0001g0135 a0001c0001t0003g0002 a0001c0001t0003g0006 others(39): Show |
67 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.647-2038dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968389 | |||||||
| chr8:56968399 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.647-2047T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968399 | |||||||
| chr8:56968651 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.647-2299G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968651 | |||||||
| chr8:56968695 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.647-2343C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968695 | |||||||
| chr8:56969362 | C | G | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3010G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969362 | |||||||
| chr8:56969362 | C | T | 1 | a0001c0001t0010g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.647-3010G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969362 | |||||||
| chr8:56969374 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0149 a0001c0001t0026g0122 |
3 | NA18962.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.647-3022A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969374 | |||||||
| chr8:56969514 | C | G | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3162G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969514 | |||||||
| chr8:56969514 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.647-3162G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969514 | |||||||
| chr8:56969520 | T | A | 36 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(33): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.647-3168A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969520 | |||||||
| chr8:56969585 | CA | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3234delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969585 | |||||||
| chr8:56969627 | G | A | 1 | a0001c0001t0004g0073 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647-3275C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969627 | |||||||
| chr8:56969748 | C | T | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-3396G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969748 | |||||||
| chr8:56969897 | T | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0078 others(19): Show |
25 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.647-3545A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969897 | |||||||
| chr8:56970015 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.647-3663G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970015 | |||||||
| chr8:56970768 | T | C | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.647-4416A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970768 | |||||||
| chr8:56970862 | C | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-4510G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970862 | |||||||
| chr8:56970863 | G | A | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.647-4511C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970863 | |||||||
| chr8:56970878 | TTCATAAA others(33): Show |
T | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.647-4566_647-4527d others(42): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970878 | |||||||
| chr8:56971269 | TA | T | 7 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0004g0063 others(4): Show |
7 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.647-4918delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971269 | |||||||
| chr8:56971269 | TAA | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(74): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.647-4919_647-4918d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971269 | |||||||
| chr8:56971305 | A | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-4953T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971305 | |||||||
| chr8:56971321 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.647-4969G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971321 | |||||||
| chr8:56971380 | G | T | 2 | a0001c0001t0004g0049 a0001c0001t0004g0053 |
2 | HG00423.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.647-5028C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971380 | |||||||
| chr8:56971422 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0104 |
2 | HG01167.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.647-5070A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971422 | |||||||
| chr8:56971504 | T | A | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-5152A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971504 | |||||||
| chr8:56971600 | G | A | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.647-5248C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971600 | |||||||
| chr8:56971619 | T | C | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-5267A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971619 | |||||||
| chr8:56971649 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.647-5297G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971649 | |||||||
| chr8:56971782 | A | AC | 79 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0027 others(76): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.647-5431dupG | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | |||||||
| chr8:56971782 | A | ACC | 53 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0028 others(50): Show |
67 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.647-5432_647-5431d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | |||||||
| chr8:56971782 | A | ACCC | 39 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0025 others(36): Show |
57 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.647-5433_647-5431d others(5): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | |||||||
| chr8:56971782 | A | ACCCC | 26 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0130 others(23): Show |
31 | HG00323.hp1 HG00597.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.647-5434_647-5431d others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | |||||||
| chr8:56971782 | A | ACCCCC | 17 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0151 others(14): Show |
20 | HG00741.hp2 HG01071.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.647-5435_647-5431d others(7): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | |||||||
| chr8:56971784 | C | CA | 4 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0092 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-5433_647-5432i others(3): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971784 | |||||||
| chr8:56971852 | T | C | 1 | a0001c0001t0030g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.647-5500A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971852 | |||||||
| chr8:56971935 | A | C | 1 | a0001c0001t0020g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.647-5583T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971935 | |||||||
| chr8:56972036 | AG | A | 46 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.647-5685delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972036 | |||||||
| chr8:56972154 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0028g0047 |
3 | HG03041.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.647-5802C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972154 | |||||||
| chr8:56972171 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.647-5819C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972171 | |||||||
| chr8:56972184 | C | A | 6 | a0001c0001t0003g0228 a0001c0001t0003g0230 a0001c0001t0003g0231 others(3): Show |
6 | HG01123.hp1 NA18965.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.647-5832G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972184 | |||||||
| chr8:56972423 | A | G | 3 | a0001c0001t0002g0212 a0001c0001t0002g0214 a0001c0001t0002g0223 |
3 | HG02451.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.646+5627T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972423 | |||||||
| chr8:56972433 | G | A | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+5617C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972433 | |||||||
| chr8:56972505 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646+5545A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972505 | |||||||
| chr8:56972512 | T | A | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646+5538A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972512 | |||||||
| chr8:56972528 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.646+5522G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972528 | |||||||
| chr8:56972565 | C | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+5485G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972565 | |||||||
| chr8:56972577 | TA | T | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+5472delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972577 | |||||||
| chr8:56972842 | T | C | 6 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0183 others(3): Show |
7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+5208A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972842 | |||||||
| chr8:56972864 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646+5186A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972864 | |||||||
| chr8:56973018 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.646+5032C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973018 | |||||||
| chr8:56973106 | G | A | 1 | a0001c0001t0015g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.646+4944C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973106 | |||||||
| chr8:56973114 | T | TCCACTGA others(33): Show |
1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646+4896_646+4935d others(42): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973114 | |||||||
| chr8:56973154 | C | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(40): Show |
58 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.646+4896G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973154 | |||||||
| chr8:56973162 | G | C | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.646+4888C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973162 | |||||||
| chr8:56973366 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.646+4684T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973366 | |||||||
| chr8:56973403 | G | T | 3 | a0001c0001t0006g0173 a0001c0001t0006g0184 a0001c0001t0006g0185 |
3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.646+4647C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973403 | |||||||
| chr8:56973475 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.646+4575G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973475 | |||||||
| chr8:56973486 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02559.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.646+4564A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973486 | |||||||
| chr8:56973657 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+4393A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973657 | |||||||
| chr8:56973666 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG00621.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.646+4384T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973666 | |||||||
| chr8:56973674 | T | C | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.646+4376A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973674 | |||||||
| chr8:56973686 | C | T | 1 | a0001c0001t0021g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646+4364G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973686 | |||||||
| chr8:56973688 | A | G | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.646+4362T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973688 | |||||||
| chr8:56973865 | A | G | 1 | a0001c0001t0003g0252 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.646+4185T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973865 | |||||||
| chr8:56974004 | C | G | 2 | a0001c0001t0016g0189 a0001c0001t0016g0197 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.646+4046G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974004 | |||||||
| chr8:56974238 | T | C | 2 | a0001c0001t0009g0017 a0001c0001t0009g0018 |
4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+3812A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974238 | |||||||
| chr8:56974385 | T | TTCAAAC | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+3664_646+3665i others(8): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974385 | |||||||
| chr8:56974564 | C | T | 2 | a0001c0001t0009g0017 a0001c0001t0009g0018 |
4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+3486G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974564 | |||||||
| chr8:56974659 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0150 |
2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.646+3391C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974659 | |||||||
| chr8:56974746 | G | T | 9 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0002g0211 others(6): Show |
12 | HG00673.hp1 HG01074.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.646+3304C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974746 | |||||||
| chr8:56974762 | A | G | 1 | a0001c0001t0030g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.646+3288T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974762 | |||||||
| chr8:56974820 | A | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+3230T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974820 | |||||||
| chr8:56975002 | G | A | 1 | a0001c0001t0003g0250 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.646+3048C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975002 | |||||||
| chr8:56975186 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.646+2864G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975186 | |||||||
| chr8:56975289 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(55): Show |
87 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.646+2761C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975289 | |||||||
| chr8:56975305 | T | C | 2 | a0001c0001t0004g0064 a0001c0001t0004g0077 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.646+2745A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975305 | |||||||
| chr8:56975474 | A | T | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646+2576T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975474 | |||||||
| chr8:56975884 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.646+2166C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975884 | |||||||
| chr8:56976042 | A | G | 1 | a0001c0001t0007g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.646+2008T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976042 | |||||||
| chr8:56976299 | T | C | 1 | a0001c0001t0004g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.646+1751A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976299 | |||||||
| chr8:56976706 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0001t0001g0168 |
4 | HG02647.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+1344C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976706 | |||||||
| chr8:56976850 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.646+1200A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976850 | |||||||
| chr8:56977104 | A | G | 11 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0183 others(8): Show |
14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.646+946T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977104 | |||||||
| chr8:56977185 | T | C | 2 | a0001c0001t0027g0045 a0001c0001t0033g0046 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.646+865A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977185 | |||||||
| chr8:56977248 | A | G | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+802T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977248 | |||||||
| chr8:56977264 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.646+786C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977264 | |||||||
| chr8:56977625 | GTAC | G | 16 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0078 others(13): Show |
18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.646+422_646+424del others(3): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977625 | |||||||
| chr8:56977631 | C | T | 16 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0078 others(13): Show |
18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.646+419G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977631 | |||||||
| chr8:56977652 | G | T | 1 | a0001c0001t0001g0012 | 3 | HG00642.hp1 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.646+398C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977652 | |||||||
| chr8:56977732 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646+318A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977732 | |||||||
| chr8:56977774 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.646+276T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977774 | |||||||
| chr8:56977776 | TG | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+273delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977776 | |||||||
| chr8:56977790 | T | C | 1 | a0001c0001t0010g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646+260A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977790 | |||||||
| chr8:56978440 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0001t0001g0168 |
4 | HG02647.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-295C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978440 | |||||||
| chr8:56978566 | C | T | 2 | a0001c0001t0009g0017 a0001c0001t0009g0018 |
4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-421G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978566 | |||||||
| chr8:56978664 | T | TA | 47 | a0001c0001t0001g0162 a0001c0001t0002g0003 a0001c0001t0002g0013 others(44): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.551-520dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978664 | |||||||
| chr8:56978680 | T | C | 46 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.551-535A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978680 | |||||||
| chr8:56978857 | T | C | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0027g0045 others(2): Show |
7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.551-712A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978857 | |||||||
| chr8:56978891 | G | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.551-746C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978891 | |||||||
| chr8:56978913 | G | C | 2 | a0001c0001t0007g0139 a0001c0001t0007g0140 |
2 | HG02040.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.551-768C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978913 | |||||||
| chr8:56979003 | C | T | 5 | a0001c0001t0004g0074 a0001c0001t0008g0019 a0001c0001t0008g0054 others(2): Show |
6 | NA18939.hp2 NA18965.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-858G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979003 | |||||||
| chr8:56979007 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.551-862T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979007 | |||||||
| chr8:56979041 | A | G | 2 | a0001c0001t0027g0045 a0001c0001t0033g0046 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.551-896T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979041 | |||||||
| chr8:56979355 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.550+680A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979355 | |||||||
| chr8:56979404 | T | C | 3 | a0001c0001t0006g0173 a0001c0001t0006g0184 a0001c0001t0006g0185 |
3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.550+631A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979404 | |||||||
| chr8:56979496 | T | C | 1 | a0001c0001t0006g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+539A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979496 | |||||||
| chr8:56979679 | T | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0001t0001g0155 others(3): Show |
7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+356A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979679 | |||||||
| chr8:56979706 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.550+329A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979706 | |||||||
| chr8:56979959 | A | G | 36 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(33): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.550+76T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979959 | |||||||
| chr8:56980235 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.388-38G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980235 | |||||||
| chr8:56980533 | A | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01167.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.388-336T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980533 | |||||||
| chr8:56980534 | A | G | 1 | a0001c0001t0004g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.388-337T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980534 | |||||||
| chr8:56980664 | G | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(250): Show |
352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.388-467C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980664 | |||||||
| chr8:56980666 | T | C | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.388-469A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980666 | |||||||
| chr8:56980751 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-554A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980751 | |||||||
| chr8:56980761 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0179 |
2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.388-564A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980761 | |||||||
| chr8:56980819 | T | C | 1 | a0001c0001t0010g0092 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-622A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TAC | 9 | a0001c0001t0001g0154 a0001c0001t0004g0067 a0001c0001t0004g0074 others(6): Show |
9 | HG00741.hp1 HG02109.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-624_388-623dup others(2): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACAC | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
7 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-626_388-623dup others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACAC | 11 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(8): Show |
14 | HG01167.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.388-628_388-623dup others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0003g0228 others(6): Show |
11 | HG01074.hp1 HG01168.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.388-630_388-623dup others(8): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACACA others(3): Show |
19 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0015 others(16): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.388-632_388-623dup others(10): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACACA others(5): Show |
9 | a0001c0001t0001g0102 a0001c0001t0003g0006 a0001c0001t0003g0237 others(6): Show |
15 | HG01516.hp2 HG02622.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.388-634_388-623dup others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACACA others(7): Show |
2 | a0001c0001t0003g0238 a0001c0001t0003g0251 |
2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.388-636_388-623dup others(14): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0223 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-638_388-623dup others(16): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATACAC | 3 | a0001c0001t0002g0199 a0001c0001t0002g0205 a0001c0001t0002g0210 |
3 | HG00408.hp1 HG00423.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.388-623_388-622ins others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATACACA others(3): Show |
16 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0039 others(13): Show |
29 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(10): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATACACA others(5): Show |
10 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0201 others(7): Show |
10 | HG02080.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATACACA others(7): Show |
12 | a0001c0001t0002g0014 a0001c0001t0002g0215 a0001c0001t0002g0216 others(9): Show |
14 | HG00673.hp1 HG01074.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(14): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATACACA others(9): Show |
3 | a0001c0001t0002g0195 a0001c0001t0002g0222 a0001c0001t0002g0227 |
3 | HG03710.hp2 HG04228.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.388-623_388-622ins others(16): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | T | TATATACA others(5): Show |
1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-623_388-622ins others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | TAC | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
9 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-624_388-623del others(2): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980819 | TACAC | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
105 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.388-626_388-623del others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | |||||||
| chr8:56980821 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.388-624G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980821 | |||||||
| chr8:56980852 | A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0211 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.388-656_388-655ins others(15): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980852 | |||||||
| chr8:56980932 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01167.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.388-735C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980932 | |||||||
| chr8:56981008 | A | AC | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-812_388-811ins others(1): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981008 | |||||||
| chr8:56981029 | G | C | 1 | a0001c0001t0035g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.388-832C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981029 | |||||||
| chr8:56981127 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(242): Show |
342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.388-930T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981127 | |||||||
| chr8:56981177 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.388-980C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981177 | |||||||
| chr8:56981324 | C | T | 46 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1127G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981324 | |||||||
| chr8:56981378 | G | A | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-1181C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981378 | |||||||
| chr8:56981407 | A | C | 1 | a0001c0001t0003g0255 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.388-1210T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981407 | |||||||
| chr8:56981636 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0022g0079 |
2 | HG01099.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.388-1439G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981636 | |||||||
| chr8:56981800 | C | A | 1 | a0001c0002t0025g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.388-1603G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981800 | |||||||
| chr8:56981901 | G | A | 1 | a0001c0001t0011g0108 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.388-1704C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981901 | |||||||
| chr8:56981917 | G | A | 1 | a0001c0001t0008g0076 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.388-1720C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981917 | |||||||
| chr8:56981944 | T | C | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0027g0045 others(2): Show |
7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-1747A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981944 | |||||||
| chr8:56982126 | C | CT | 14 | a0001c0001t0001g0057 a0001c0001t0001g0111 a0001c0001t0001g0116 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-1930dupA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982126 | |||||||
| chr8:56982126 | C | CTT | 5 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0184 others(2): Show |
6 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-1931_388-1930d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982126 | |||||||
| chr8:56982128 | T | C | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0227 |
3 | NA18969.hp2 NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.388-1931A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982128 | |||||||
| chr8:56982380 | C | G | 1 | a0001c0001t0030g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.388-2183G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982380 | |||||||
| chr8:56982413 | G | A | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-2216C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982413 | |||||||
| chr8:56982510 | C | T | 5 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0183 others(2): Show |
5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-2313G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982510 | |||||||
| chr8:56982519 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.388-2322A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982519 | |||||||
| chr8:56982565 | G | A | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.388-2368C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982565 | |||||||
| chr8:56982580 | G | A | 18 | a0001c0001t0003g0009 a0001c0001t0003g0228 a0001c0001t0003g0229 others(15): Show |
24 | HG01074.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-2383C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982580 | |||||||
| chr8:56982610 | A | T | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.388-2413T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982610 | |||||||
| chr8:56982642 | TG | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.388-2446delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982642 | |||||||
| chr8:56982695 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.388-2498A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982695 | |||||||
| chr8:56982760 | T | A | 1 | a0001c0002t0024g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-2563A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982760 | |||||||
| chr8:56982872 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-2675A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982872 | |||||||
| chr8:56982916 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
7 | HG01258.hp1 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-2719G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982916 | |||||||
| chr8:56983049 | C | T | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-2852G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983049 | |||||||
| chr8:56983238 | C | T | 6 | a0001c0001t0006g0173 a0001c0001t0006g0184 a0001c0001t0006g0185 others(3): Show |
6 | HG00741.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-3041G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983238 | |||||||
| chr8:56983542 | C | T | 2 | a0001c0001t0027g0045 a0001c0001t0033g0046 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.388-3345G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983542 | |||||||
| chr8:56983659 | A | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG00099.hp2 HG00738.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-3462T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983659 | |||||||
| chr8:56983876 | G | A | 3 | a0001c0001t0006g0173 a0001c0001t0006g0184 a0001c0001t0006g0185 |
3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.388-3679C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983876 | |||||||
| chr8:56983999 | G | A | 3 | a0001c0002t0024g0181 a0001c0002t0025g0182 a0001c0002t0037g0256 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.388-3802C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983999 | |||||||
| chr8:56984076 | T | C | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-3879A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984076 | |||||||
| chr8:56984123 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02559.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.388-3926C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984123 | |||||||
| chr8:56984805 | TATC | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.388-4611_388-4609d others(5): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984805 | |||||||
| chr8:56984834 | T | A | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-4637A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984834 | |||||||
| chr8:56984861 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0011g0026 others(1): Show |
5 | HG00323.hp2 HG01081.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4664G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984861 | |||||||
| chr8:56984979 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.388-4782G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984979 | |||||||
| chr8:56985100 | A | G | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-4903T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985100 | |||||||
| chr8:56985133 | T | C | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4936A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985133 | |||||||
| chr8:56985153 | G | A | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4956C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985153 | |||||||
| chr8:56985200 | C | A | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-5003G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985200 | |||||||
| chr8:56985316 | T | C | 2 | a0001c0001t0027g0045 a0001c0001t0033g0046 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.388-5119A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985316 | |||||||
| chr8:56985385 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388-5188A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985385 | |||||||
| chr8:56985454 | C | CACCCTGG others(3): Show |
1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5258_388-5257i others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985454 | |||||||
| chr8:56985607 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5410A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985607 | |||||||
| chr8:56985679 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5482A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985679 | |||||||
| chr8:56985796 | G | A | 99 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0013 others(96): Show |
142 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.388-5599C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985796 | |||||||
| chr8:56985818 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.388-5621A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985818 | |||||||
| chr8:56985835 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5638C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985835 | |||||||
| chr8:56985918 | C | A | 3 | a0001c0001t0006g0173 a0001c0001t0006g0184 a0001c0001t0006g0185 |
3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.388-5721G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985918 | |||||||
| chr8:56985941 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5744G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985941 | |||||||
| chr8:56986018 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.388-5821G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986018 | |||||||
| chr8:56986069 | T | C | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-5872A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986069 | |||||||
| chr8:56986081 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.388-5884C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986081 | |||||||
| chr8:56986361 | G | A | 47 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.388-6164C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986361 | |||||||
| chr8:56986379 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-6182T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986379 | |||||||
| chr8:56986408 | T | C | 1 | a0001c0002t0025g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.388-6211A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986408 | |||||||
| chr8:56986411 | G | T | 1 | a0001c0001t0004g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.388-6214C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986411 | |||||||
| chr8:56986579 | C | A | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-6382G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986579 | |||||||
| chr8:56986682 | A | G | 16 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0078 others(13): Show |
18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.388-6485T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986682 | |||||||
| chr8:56986739 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6460A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986739 | |||||||
| chr8:56986740 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6459T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986740 | |||||||
| chr8:56986742 | T | C | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+6457A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986742 | |||||||
| chr8:56986769 | A | G | 1 | a0001c0001t0002g0205 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.387+6430T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986769 | |||||||
| chr8:56986809 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6390A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986809 | |||||||
| chr8:56986810 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6389C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986810 | |||||||
| chr8:56986846 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6353C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986846 | |||||||
| chr8:56986847 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6352G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986847 | |||||||
| chr8:56986982 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.387+6217A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986982 | |||||||
| chr8:56987052 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6147C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987052 | |||||||
| chr8:56987054 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6145T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987054 | |||||||
| chr8:56987056 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6143C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987056 | |||||||
| chr8:56987262 | T | C | 2 | a0001c0001t0016g0189 a0001c0001t0016g0197 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.387+5937A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987262 | |||||||
| chr8:56987311 | T | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+5888A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987311 | |||||||
| chr8:56987406 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5793T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987406 | |||||||
| chr8:56987566 | C | T | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+5633G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987566 | |||||||
| chr8:56987616 | C | A | 84 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(81): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.387+5583G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987616 | |||||||
| chr8:56987674 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.387+5525A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987674 | |||||||
| chr8:56987731 | C | CT | 54 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0105 others(51): Show |
68 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.387+5467dupA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987731 | |||||||
| chr8:56987731 | CT | C | 39 | a0001c0001t0001g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(36): Show |
65 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.387+5467delA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987731 | |||||||
| chr8:56987733 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5466A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987733 | |||||||
| chr8:56987736 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.387+5463A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987736 | |||||||
| chr8:56987797 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5402G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987797 | |||||||
| chr8:56987798 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5401C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987798 | |||||||
| chr8:56987803 | A | C | 36 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(33): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+5396T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987803 | |||||||
| chr8:56987885 | C | T | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+5314G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987885 | |||||||
| chr8:56987994 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.387+5205G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987994 | |||||||
| chr8:56988069 | C | T | 2 | a0001c0001t0016g0189 a0001c0001t0016g0197 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.387+5130G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988069 | |||||||
| chr8:56988132 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.387+5067A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988132 | |||||||
| chr8:56988134 | G | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(80): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.387+5065C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988134 | |||||||
| chr8:56988414 | T | C | 2 | a0001c0001t0002g0205 a0001c0001t0002g0210 |
2 | HG00423.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.387+4785A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988414 | |||||||
| chr8:56988541 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.387+4658A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988541 | |||||||
| chr8:56988619 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.387+4580A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988619 | |||||||
| chr8:56988684 | G | A | 1 | a0001c0001t0028g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.387+4515C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988684 | |||||||
| chr8:56988697 | AGATGTTT others(30): Show |
A | 1 | a0001c0001t0004g0050 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.387+4465_387+4501d others(39): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988697 | |||||||
| chr8:56988868 | T | C | 2 | a0001c0001t0004g0021 a0001c0001t0004g0022 |
4 | NA18967.hp1 NA18975.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+4331A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988868 | |||||||
| chr8:56988910 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(217): Show |
304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.387+4289G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988910 | |||||||
| chr8:56988944 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.387+4255G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988944 | |||||||
| chr8:56989200 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0166 a0001c0001t0001g0176 |
4 | HG01109.hp2 HG02055.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3999G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989200 | |||||||
| chr8:56989209 | TAA | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3988_387+3989d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989209 | |||||||
| chr8:56989350 | C | T | 5 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0183 others(2): Show |
5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+3849G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989350 | |||||||
| chr8:56989358 | C | T | 1 | a0001c0001t0030g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.387+3841G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989358 | |||||||
| chr8:56989372 | T | TA | 7 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(4): Show |
7 | HG00423.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+3826dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989372 | |||||||
| chr8:56989372 | TA | T | 99 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0013 others(96): Show |
142 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.387+3826delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989372 | |||||||
| chr8:56989443 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.387+3756A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989443 | |||||||
| chr8:56989454 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.387+3745C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989454 | |||||||
| chr8:56989767 | A | C | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+3432T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989767 | |||||||
| chr8:56989829 | A | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3370T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989829 | |||||||
| chr8:56989872 | A | G | 11 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0230 others(8): Show |
11 | HG01123.hp1 NA18941.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.387+3327T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989872 | |||||||
| chr8:56989938 | G | T | 1 | a0001c0002t0024g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387+3261C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989938 | |||||||
| chr8:56990050 | T | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(34): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3149A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990050 | |||||||
| chr8:56990050 | T | C | 1 | a0001c0001t0008g0076 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+3149A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990050 | |||||||
| chr8:56990397 | T | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.387+2802A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990397 | |||||||
| chr8:56990425 | G | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.387+2774C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990425 | |||||||
| chr8:56990534 | A | C | 36 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(33): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+2665T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990534 | |||||||
| chr8:56990639 | G | T | 1 | a0001c0001t0019g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+2560C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990639 | |||||||
| chr8:56990650 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | NA18956.hp1 NA18983.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.387+2549G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990650 | |||||||
| chr8:56990798 | C | A | 6 | a0001c0001t0006g0173 a0001c0001t0006g0180 a0001c0001t0006g0183 others(3): Show |
7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+2401G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990798 | |||||||
| chr8:56990870 | A | G | 1 | a0001c0001t0003g0244 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.387+2329T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990870 | |||||||
| chr8:56991075 | A | G | 2 | a0001c0001t0009g0017 a0001c0001t0009g0018 |
4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2124T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991075 | |||||||
| chr8:56991326 | G | T | 3 | a0001c0001t0027g0045 a0001c0001t0028g0047 a0001c0001t0033g0046 |
3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.387+1873C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991326 | |||||||
| chr8:56991329 | T | TTCAA | 3 | a0001c0001t0001g0087 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG01109.hp1 HG01978.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.387+1866_387+1869d others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991329 | |||||||
| chr8:56991618 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.387+1581G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991618 | |||||||
| chr8:56992013 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+1186C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992013 | |||||||
| chr8:56992042 | G | C | 1 | a0001c0001t0004g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.387+1157C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992042 | |||||||
| chr8:56992142 | A | G | 5 | a0001c0001t0010g0088 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1057T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992142 | |||||||
| chr8:56992241 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+958G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992241 | |||||||
| chr8:56992257 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.387+942C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992257 | |||||||
| chr8:56992281 | C | A | 46 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.387+918G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992281 | |||||||
| chr8:56992404 | T | G | 23 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0002g0193 others(20): Show |
26 | HG00673.hp1 HG01074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.387+795A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992404 | |||||||
| chr8:56992452 | A | AATCCAAA others(30): Show |
1 | a0001c0001t0004g0050 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.387+710_387+746dup others(37): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992452 | |||||||
| chr8:56992640 | T | G | 38 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.387+559A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992640 | |||||||
| chr8:56992641 | T | A | 38 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.387+558A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992641 | |||||||
| chr8:56992688 | A | AC | 27 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0001g0080 others(24): Show |
29 | HG00423.hp2 HG01099.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.387+510dupG | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992688 | |||||||
| chr8:56992714 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(217): Show |
304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.387+485C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992714 | |||||||
| chr8:56992724 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+475T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992724 | |||||||
| chr8:56992738 | C | T | 46 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0014 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.387+461G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992738 | |||||||
| chr8:56992791 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.387+408C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992791 | |||||||
| chr8:56992813 | C | A | 13 | a0001c0001t0006g0180 a0001c0001t0006g0183 a0001c0001t0006g0184 others(10): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+386G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992813 | |||||||
| chr8:56992941 | C | G | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0027g0045 others(2): Show |
7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+258G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992941 | |||||||
| chr8:56992986 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.387+213C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992986 | |||||||
| chr8:56993138 | G | C | 25 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0009 others(22): Show |
50 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.387+61C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56993138 |