Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4686 |
| ensemblid | ENSG00000136937.13 |
| hgncid | 7658 |
| symbol | NCBP1 |
| name | nuclear cap binding protein subunit 1 |
| refseq_nuc | NM_002486.5 |
| refseq_prot | NP_002477.1 |
| ensembl_nuc | ENST00000375147.8 |
| ensembl_prot | ENSP00000364289.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97633821 |
| end | 97673748 |
| strand | + |
| ver | v1.2 |
| region | chr9:97633821-97673748 |
| region5000 | chr9:97628821-97678748 |
| regionname0 | NCBP1_chr9_97633821_97673748 |
| regionname5000 | NCBP1_chr9_97628821_97678748 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 790 | 360 | 89 | 62 | 154 | 13 | 40 | 120 | NCBP1_chr9_97628821_97678748 | NCBP1 | MSRRR others(785): Show |
chr9 | 97628821 | 97678748 |
| a0002 | 0/0 | 790 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | MSRRR others(785): Show |
chr9 | 97628821 | 97678748 |
| a0003 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | MSRRR others(785): Show |
chr9 | 97628821 | 97678748 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2370 | 268 | 36 | 45 | 134 | 13 | 38 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0002 | 0/0 | 2370 | 58 | 26 | 12 | 19 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0003 | 0/0 | 2370 | 15 | 14 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0004 | 0/0 | 2370 | 6 | 6 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0005 | 0/0 | 2370 | 6 | 4 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0007 | 0/0 | 2370 | 2 | 1 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0008 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0010 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0011 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0012 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0001c0013 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0002c0006 | 0/0 | 2370 | 3 | 0 | 2 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 | ||
| a0003c0009 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | ATGTC others(2365): Show |
chr9 | 97628821 | 97678748 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4983 | 245 | 35 | 42 | 124 | 11 | 31 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0003 | 0/0 | 4980 | 14 | 0 | 2 | 4 | 2 | 6 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4975): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0008 | 0/0 | 4983 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0009 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0010 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0011 | 0/0 | 4983 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0014 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0016 | 0/0 | 4983 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0001t0019 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0002t0002 | 0/0 | 4983 | 42 | 11 | 11 | 19 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0002t0005 | 0/0 | 4983 | 13 | 12 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0002t0013 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0002t0017 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0002t0018 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0003t0004 | 0/0 | 4978 | 15 | 14 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4973): Show |
chr9 | 97628821 | 97678748 |
| a0001c0004t0007 | 0/0 | 4987 | 5 | 5 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4982): Show |
chr9 | 97628821 | 97678748 |
| a0001c0004t0012 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0005t0006 | 0/0 | 4982 | 6 | 4 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4977): Show |
chr9 | 97628821 | 97678748 |
| a0001c0007t0001 | 0/0 | 4983 | 2 | 1 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0008t0001 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0010t0015 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0011t0003 | 0/0 | 4980 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4975): Show |
chr9 | 97628821 | 97678748 |
| a0001c0012t0002 | 0/0 | 4983 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0001c0013t0002 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0002c0006t0001 | 0/0 | 4983 | 3 | 0 | 2 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| a0003c0009t0002 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | AGACA others(4978): Show |
chr9 | 97628821 | 97678748 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0014 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0011g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0014g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0016g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0013g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0002t0018g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0004t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0005t0006g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0005t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0005t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0005t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0007t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0008t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0010t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0011t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0012t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0001c0013t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0002c0006t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0002c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0002c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| a0003c0009t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | GBR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00597 | hp2 | a0001 | c0013 | t0002 | g0056 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00621 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01081 | hp2 | a0001 | c0007 | t0001 | g0040 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01109 | hp2 | a0001 | c0005 | t0006 | g0112 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01167 | hp2 | a0002 | c0006 | t0001 | g0263 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01168 | hp1 | a0002 | c0006 | t0001 | g0244 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01243 | hp1 | a0001 | c0005 | t0006 | g0228 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0069 | AMR | PUR | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0204 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01515 | hp1 | a0002 | c0006 | t0001 | g0264 | EUR | IBS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0067 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0091 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01952 | hp1 | a0001 | c0003 | t0004 | g0009 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02145 | hp1 | a0001 | c0002 | t0017 | g0062 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02148 | hp2 | a0001 | c0012 | t0002 | g0052 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CDX | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CDX | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0019 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02258 | hp1 | a0001 | c0002 | t0013 | g0096 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02280 | hp2 | a0001 | c0004 | t0012 | g0073 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0086 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02647 | hp1 | a0001 | c0010 | t0015 | g0165 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02717 | hp1 | a0001 | c0003 | t0004 | g0085 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02717 | hp2 | a0001 | c0008 | t0001 | g0206 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02723 | hp1 | a0001 | c0005 | t0006 | g0017 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0094 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0040 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0071 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02818 | hp2 | a0001 | c0005 | t0006 | g0017 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02886 | hp2 | a0001 | c0005 | t0006 | g0275 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02895 | hp2 | a0001 | c0005 | t0006 | g0017 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02922 | hp1 | a0001 | c0004 | t0007 | g0074 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0009 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02976 | hp1 | a0003 | c0009 | t0002 | g0087 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0020 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03041 | hp1 | a0001 | c0003 | t0004 | g0090 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0070 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03098 | hp1 | a0001 | c0004 | t0007 | g0075 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0066 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0063 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0093 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0095 | AFR | ESN | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03834 | hp2 | a0001 | c0011 | t0003 | g0143 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03942 | hp2 | a0001 | c0001 | t0016 | g0105 | SAS | BEB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18522 | hp2 | a0001 | c0002 | t0005 | g0065 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18977 | hp1 | a0001 | c0001 | t0014 | g0005 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0248 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | LWK | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | LWK | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19240 | hp1 | a0001 | c0003 | t0004 | g0009 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA19240 | hp2 | a0001 | c0004 | t0007 | g0076 | AFR | YRI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20129 | hp1 | a0001 | c0003 | t0004 | g0089 | AFR | ASW | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20129 | hp2 | a0001 | c0003 | t0004 | g0079 | AFR | ASW | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | TSI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | GIH | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0077 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0072 | AFR | MSL | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG06807 | hp1 | a0001 | c0004 | t0007 | g0078 | AFR | USA | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | USA | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA20300 | hp2 | a0001 | c0003 | t0004 | g0092 | AFR | USA | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA21309 | hp1 | a0001 | c0002 | t0018 | g0082 | AFR | LWK | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0122 | AFR | LWK | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0205 | REF | REF | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0014 | REF | REF | NCBP1_chr9_97628821_97678748 | NCBP1 | chr9 | 97628821 | 97678748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97656049 | C | T | 1 | a0002 | 3 | HG01167.hp2 HG01168.hp1 HG01515.hp1 |
missense_variant | MODERATE | c.1337C>T | p.Pro446Leu | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/23 | 1398/4983 | 1337/2373 | 446/790 | chr9 | 97656049 | |||
| chr9:97666830 | A | C | 1 | a0003 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1969A>C | p.Lys657Gln | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/23 | 2030/4983 | 1969/2373 | 657/790 | chr9 | 97666830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97643345 | T | C | 1 | a0001c0003 | 15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
synonymous_variant | LOW | c.366T>C | p.Asn122Asn | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/23 | 427/4983 | 366/2373 | 122/790 | chr9 | 97643345 | |||
| chr9:97645158 | C | T | 1 | a0001c0013 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.423C>T | p.Ala141Ala | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 5/23 | 484/4983 | 423/2373 | 141/790 | chr9 | 97645158 | |||
| chr9:97645652 | G | A | 1 | a0001c0008 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.531G>A | p.Leu177Leu | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/23 | 592/4983 | 531/2373 | 177/790 | chr9 | 97645652 | |||
| chr9:97647528 | A | G | 1 | a0001c0012 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.648A>G | p.Val216Val | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 7/23 | 709/4983 | 648/2373 | 216/790 | chr9 | 97647528 | |||
| chr9:97653887 | A | G | 1 | a0001c0005 | 6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.1149A>G | p.Gln383Gln | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/23 | 1210/4983 | 1149/2373 | 383/790 | chr9 | 97653887 | |||
| chr9:97658694 | G | A | 6 | a0001c0002 a0001c0003 a0001c0004 others(3): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
synonymous_variant | LOW | c.1428G>A | p.Leu476Leu | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/23 | 1489/4983 | 1428/2373 | 476/790 | chr9 | 97658694 | |||
| chr9:97658739 | T | C | 1 | a0001c0010 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1473T>C | p.Ser491Ser | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/23 | 1534/4983 | 1473/2373 | 491/790 | chr9 | 97658739 | |||
| chr9:97660965 | T | C | 1 | a0001c0004 | 6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
synonymous_variant | LOW | c.1497T>C | p.Ser499Ser | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/23 | 1558/4983 | 1497/2373 | 499/790 | chr9 | 97660965 | |||
| chr9:97668860 | C | T | 1 | a0001c0007 | 2 | HG01081.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.2031C>T | p.Asp677Asp | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/23 | 2092/4983 | 2031/2373 | 677/790 | chr9 | 97668860 | |||
| chr9:97669637 | T | C | 1 | a0001c0011 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.2190T>C | p.Thr730Thr | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/23 | 2251/4983 | 2190/2373 | 730/790 | chr9 | 97669637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97671360 | G | A | 1 | a0001c0001t0009 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 161 | chr9 | 97671360 | ||||||
| chr9:97671609 | A | G | 1 | a0001c0001t0019 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 410 | chr9 | 97671609 | ||||||
| chr9:97671901 | T | G | 1 | a0001c0001t0008 | 3 | NA18955.hp1 NA18965.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*702T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 702 | chr9 | 97671901 | ||||||
| chr9:97671957 | C | G | 1 | a0001c0002t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 758 | chr9 | 97671957 | ||||||
| chr9:97672016 | G | A | 1 | a0001c0001t0010 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 817 | chr9 | 97672016 | ||||||
| chr9:97672022 | G | A | 1 | a0001c0001t0011 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 823 | chr9 | 97672022 | ||||||
| chr9:97672276 | GTGT | G | 2 | a0001c0001t0003 a0001c0011t0003 |
15 | HG00140.hp1 HG00438.hp1 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1084_*1086delTGT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1084 | INFO_REALIGN_3_PRIME | chr9 | 97672276 | |||||
| chr9:97672347 | C | T | 3 | a0001c0002t0005 a0001c0002t0017 a0001c0002t0018 |
15 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1148C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1148 | chr9 | 97672347 | ||||||
| chr9:97672803 | GATTTT | G | 1 | a0001c0003t0004 | 15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1610_*1614delATTT others(1): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1610 | INFO_REALIGN_3_PRIME | chr9 | 97672803 | |||||
| chr9:97672855 | G | A | 11 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0013 others(8): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1656G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1656 | chr9 | 97672855 | ||||||
| chr9:97672899 | C | T | 1 | a0001c0002t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1700C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1700 | chr9 | 97672899 | ||||||
| chr9:97673134 | GA | G | 1 | a0001c0005t0006 | 6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1943delA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1943 | INFO_REALIGN_3_PRIME | chr9 | 97673134 | |||||
| chr9:97673190 | G | GGTAA | 1 | a0001c0004t0007 | 5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1994_*1997dupAAGT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 1998 | INFO_REALIGN_3_PRIME | chr9 | 97673190 | |||||
| chr9:97673263 | C | T | 1 | a0001c0002t0005 | 13 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2064C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 2064 | chr9 | 97673263 | ||||||
| chr9:97673454 | A | G | 1 | a0001c0001t0016 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2255A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 2255 | chr9 | 97673454 | ||||||
| chr9:97673473 | C | T | 1 | a0001c0010t0015 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2274C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 2274 | chr9 | 97673473 | ||||||
| chr9:97673480 | C | T | 1 | a0001c0001t0014 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2281C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 2281 | chr9 | 97673480 | ||||||
| chr9:97673741 | A | G | 2 | a0001c0004t0007 a0001c0004t0012 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2542A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 23/23 | 2542 | chr9 | 97673741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97634040 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.34+125G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634040 | |||||||
| chr9:97634054 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.34+139T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634054 | |||||||
| chr9:97634173 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02809.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+258C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634173 | |||||||
| chr9:97634386 | G | T | 1 | a0001c0001t0001g0287 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.34+471G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634386 | |||||||
| chr9:97634457 | C | T | 1 | a0001c0002t0013g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.34+542C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634457 | |||||||
| chr9:97634918 | T | G | 1 | a0001c0002t0013g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.34+1003T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634918 | |||||||
| chr9:97634959 | T | A | 1 | a0001c0001t0003g0097 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.34+1044T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97634959 | |||||||
| chr9:97635382 | C | T | 2 | a0001c0002t0002g0023 a0001c0002t0002g0095 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.34+1467C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635382 | |||||||
| chr9:97635414 | C | CTTTTT | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.34+1509_34+1513dup others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97635414 | ||||||
| chr9:97635414 | C | CTTTTTT | 29 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0080 others(26): Show |
33 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.34+1508_34+1513dup others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97635414 | ||||||
| chr9:97635414 | C | CTTTTTTT | 12 | a0001c0002t0002g0088 a0001c0002t0005g0086 a0001c0003t0004g0009 others(9): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+1507_34+1513dup others(7): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97635414 | ||||||
| chr9:97635414 | CT | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0099 others(13): Show |
18 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.34+1513delT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97635414 | ||||||
| chr9:97635426 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.34+1511T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635426 | |||||||
| chr9:97635538 | G | C | 1 | a0001c0003t0004g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.34+1623G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635538 | |||||||
| chr9:97635567 | C | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.34+1652C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635567 | |||||||
| chr9:97635572 | G | A | 1 | a0001c0002t0017g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.34+1657G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635572 | |||||||
| chr9:97635827 | G | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.34+1912G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635827 | |||||||
| chr9:97635972 | T | C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(37): Show |
51 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.34+2057T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97635972 | |||||||
| chr9:97636067 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2152C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636067 | |||||||
| chr9:97636068 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2153A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636068 | |||||||
| chr9:97636192 | C | CA | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.34+2277_34+2278ins others(1): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636192 | |||||||
| chr9:97636262 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.34+2347A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636262 | |||||||
| chr9:97636417 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2502T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636417 | |||||||
| chr9:97636429 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2514T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636429 | |||||||
| chr9:97636430 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2515A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636430 | |||||||
| chr9:97636431 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2516T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636431 | |||||||
| chr9:97636434 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2519A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636434 | |||||||
| chr9:97636450 | TAAACTAT others(9): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2536_34+2551del others(16): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636450 | |||||||
| chr9:97636464 | A | G | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.34+2549A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636464 | |||||||
| chr9:97636469 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2554T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636469 | |||||||
| chr9:97636476 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2561T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636476 | |||||||
| chr9:97636478 | T | A | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.34+2563T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636478 | |||||||
| chr9:97636480 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2565T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636480 | |||||||
| chr9:97636488 | A | ATATAAAT others(14): Show |
1 | a0001c0002t0002g0048 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.34+2599_34+2619dup others(21): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636488 | ||||||
| chr9:97636488 | ATATAAAT others(14): Show |
A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(124): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.34+2599_34+2619del others(21): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636488 | ||||||
| chr9:97636493 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2578A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636493 | |||||||
| chr9:97636508 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2593A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636508 | |||||||
| chr9:97636509 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.34+2594T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636509 | |||||||
| chr9:97636637 | C | CAT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(23): Show |
32 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.34+2758_34+2759dup others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | C | CATAT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0041 others(17): Show |
27 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.34+2756_34+2759dup others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | C | CATATAT | 22 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0137 others(19): Show |
27 | HG00408.hp1 HG00438.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.34+2754_34+2759dup others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | C | CATATATA others(1): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0276 a0001c0001t0001g0277 others(6): Show |
10 | HG03669.hp1 HG04204.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+2752_34+2759dup others(8): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | C | CATATATA others(3): Show |
5 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0001g0283 others(2): Show |
5 | HG00544.hp2 NA19062.hp2 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+2750_34+2759dup others(10): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0285 |
3 | NA18966.hp1 NA18992.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.34+2746_34+2759dup others(14): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CAT | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0037 others(54): Show |
63 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.34+2758_34+2759del others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATAT | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0029 others(25): Show |
37 | HG00438.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.34+2756_34+2759del others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATAT | C | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(28): Show |
46 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.34+2754_34+2759del others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(1): Show |
C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0100 others(10): Show |
19 | HG00099.hp1 HG01099.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.34+2752_34+2759del others(8): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(3): Show |
C | 8 | a0001c0001t0001g0099 a0001c0002t0002g0080 a0001c0002t0002g0081 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+2750_34+2759del others(10): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(5): Show |
C | 4 | a0001c0002t0002g0023 a0001c0002t0002g0088 a0001c0002t0002g0095 others(1): Show |
5 | HG01891.hp1 HG02976.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+2748_34+2759del others(12): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(7): Show |
C | 7 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+2746_34+2759del others(14): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(9): Show |
C | 6 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG02135.hp1 HG03471.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+2744_34+2759del others(16): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(11): Show |
C | 12 | a0001c0001t0001g0229 a0001c0002t0005g0019 a0001c0002t0005g0063 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.34+2742_34+2759del others(18): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636637 | CATATATA others(13): Show |
C | 1 | a0001c0005t0006g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.34+2740_34+2759del others(20): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97636637 | ||||||
| chr9:97636645 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+2730T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636645 | |||||||
| chr9:97636673 | T | A | 1 | a0001c0002t0002g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.34+2758T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636673 | |||||||
| chr9:97636705 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.34+2790G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636705 | |||||||
| chr9:97636773 | G | A | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.34+2858G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636773 | |||||||
| chr9:97636850 | G | A | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(37): Show |
51 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.34+2935G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636850 | |||||||
| chr9:97636918 | G | A | 2 | a0001c0002t0002g0088 a0003c0009t0002g0087 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.34+3003G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636918 | |||||||
| chr9:97636998 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+3083A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97636998 | |||||||
| chr9:97637106 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+3191G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637106 | |||||||
| chr9:97637107 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+3192A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637107 | |||||||
| chr9:97637123 | A | G | 55 | a0001c0001t0001g0167 a0001c0001t0001g0224 a0001c0001t0001g0256 others(52): Show |
74 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.34+3208A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637123 | |||||||
| chr9:97637183 | A | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.34+3268A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637183 | |||||||
| chr9:97637190 | A | AG | 26 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+3281dupG | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97637190 | ||||||
| chr9:97637195 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+3280G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637195 | |||||||
| chr9:97637223 | G | A | 1 | a0001c0011t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.34+3308G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637223 | |||||||
| chr9:97637358 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-3436T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637358 | |||||||
| chr9:97637360 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-3434A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637360 | |||||||
| chr9:97637361 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-3433C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637361 | |||||||
| chr9:97637371 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.35-3423T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637371 | |||||||
| chr9:97637401 | T | G | 61 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(58): Show |
81 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.35-3393T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637401 | |||||||
| chr9:97637421 | T | G | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.35-3373T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637421 | |||||||
| chr9:97637453 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0125 others(5): Show |
10 | HG00741.hp1 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.35-3341A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637453 | |||||||
| chr9:97637630 | C | CCT | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.35-3163_35-3162dup others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97637630 | ||||||
| chr9:97637774 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-3020A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637774 | |||||||
| chr9:97637807 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.35-2987T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637807 | |||||||
| chr9:97637852 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(187): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.35-2942G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97637852 | |||||||
| chr9:97638002 | AT | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(62): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.35-2791delT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638002 | |||||||
| chr9:97638014 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-2780T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638014 | |||||||
| chr9:97638016 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-2778A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638016 | |||||||
| chr9:97638017 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-2777T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638017 | |||||||
| chr9:97638284 | A | G | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-2510A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638284 | |||||||
| chr9:97638362 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0168 a0001c0001t0001g0193 |
5 | NA18747.hp1 NA18968.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-2432T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638362 | |||||||
| chr9:97638606 | A | T | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.35-2188A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638606 | |||||||
| chr9:97638619 | T | C | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.35-2175T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638619 | |||||||
| chr9:97638753 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.35-2041G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638753 | |||||||
| chr9:97638756 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.35-2038A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638756 | |||||||
| chr9:97638823 | A | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.35-1971A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638823 | |||||||
| chr9:97638989 | C | T | 2 | a0001c0002t0002g0021 a0001c0002t0002g0083 |
3 | HG03225.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.35-1805C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97638989 | |||||||
| chr9:97639084 | T | C | 2 | a0001c0002t0002g0049 a0001c0002t0002g0053 |
2 | NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.35-1710T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639084 | |||||||
| chr9:97639179 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.35-1615C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639179 | |||||||
| chr9:97639179 | C | T | 17 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0083 others(14): Show |
23 | HG01891.hp1 HG01891.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.35-1615C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639179 | |||||||
| chr9:97639291 | C | A | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.35-1503C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639291 | |||||||
| chr9:97639339 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.35-1455A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639339 | |||||||
| chr9:97639514 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.35-1280A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639514 | |||||||
| chr9:97639831 | A | C | 53 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(50): Show |
70 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.35-963A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639831 | |||||||
| chr9:97639831 | A | T | 9 | a0001c0003t0004g0009 a0001c0003t0004g0022 a0001c0003t0004g0085 others(6): Show |
12 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.35-963A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639831 | |||||||
| chr9:97639880 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.35-914A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639880 | |||||||
| chr9:97639908 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0114 a0001c0001t0001g0117 |
4 | HG01358.hp2 HG01515.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-886C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639908 | |||||||
| chr9:97639943 | CAT | C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(37): Show |
51 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.35-849_35-848delTA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 97639943 | ||||||
| chr9:97639959 | A | G | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-835A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97639959 | |||||||
| chr9:97640079 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18953.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.35-715T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97640079 | |||||||
| chr9:97640317 | C | T | 1 | a0002c0006t0001g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.35-477C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97640317 | |||||||
| chr9:97640444 | G | A | 6 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0083 others(3): Show |
8 | HG01891.hp1 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.35-350G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97640444 | |||||||
| chr9:97640592 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.35-202G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 1/22 | chr9 | 97640592 | |||||||
| chr9:97640908 | G | A | 1 | a0001c0005t0006g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+26G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97640908 | |||||||
| chr9:97640944 | T | A | 2 | a0001c0002t0002g0047 a0001c0002t0002g0084 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.123+62T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97640944 | |||||||
| chr9:97640985 | G | T | 1 | a0001c0001t0003g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+103G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97640985 | |||||||
| chr9:97641110 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0193 |
2 | NA18747.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.123+228G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97641110 | |||||||
| chr9:97641287 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-275C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97641287 | |||||||
| chr9:97641443 | GTAATGAT others(12): Show |
G | 2 | a0001c0002t0002g0088 a0003c0009t0002g0087 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124-118_124-100del others(19): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97641443 | |||||||
| chr9:97641463 | G | C | 2 | a0001c0002t0002g0088 a0003c0009t0002g0087 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124-99G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 2/22 | chr9 | 97641463 | |||||||
| chr9:97641811 | C | T | 2 | a0001c0002t0002g0023 a0001c0002t0002g0095 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.224+149C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97641811 | |||||||
| chr9:97642066 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.224+404G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642066 | |||||||
| chr9:97642156 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+494G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642156 | |||||||
| chr9:97642397 | T | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.224+735T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642397 | |||||||
| chr9:97642436 | C | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00099.hp2 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.225-768C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642436 | |||||||
| chr9:97642507 | C | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.225-697C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642507 | |||||||
| chr9:97642597 | T | G | 1 | a0001c0001t0001g0286 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.225-607T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642597 | |||||||
| chr9:97642661 | A | G | 2 | a0001c0001t0001g0118 a0001c0002t0018g0082 |
2 | HG02155.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.225-543A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642661 | |||||||
| chr9:97642944 | A | T | 1 | a0001c0002t0005g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.225-260A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642944 | |||||||
| chr9:97642956 | A | G | 12 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.225-248A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97642956 | |||||||
| chr9:97643183 | T | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.225-21T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3/22 | chr9 | 97643183 | |||||||
| chr9:97643671 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.381+311T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97643671 | |||||||
| chr9:97643731 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00099.hp2 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.381+371G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97643731 | |||||||
| chr9:97643772 | A | G | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.381+412A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97643772 | |||||||
| chr9:97643994 | G | T | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+634G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97643994 | |||||||
| chr9:97644052 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.381+692A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644052 | |||||||
| chr9:97644204 | G | A | 2 | a0001c0003t0004g0020 a0001c0003t0004g0079 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+844G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644204 | |||||||
| chr9:97644255 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.382-862C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644255 | |||||||
| chr9:97644283 | C | T | 1 | a0001c0012t0002g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.382-834C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644283 | |||||||
| chr9:97644647 | G | GAAAATTA others(12): Show |
1 | a0001c0003t0004g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.382-466_382-448dup others(19): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 97644647 | ||||||
| chr9:97644769 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.382-348T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644769 | |||||||
| chr9:97644844 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.382-273G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644844 | |||||||
| chr9:97644872 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.382-245G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644872 | |||||||
| chr9:97644936 | G | A | 1 | a0001c0005t0006g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.382-181G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644936 | |||||||
| chr9:97644974 | A | G | 16 | a0001c0002t0002g0047 a0001c0002t0002g0084 a0001c0002t0005g0019 others(13): Show |
17 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.382-143A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 4/22 | chr9 | 97644974 | |||||||
| chr9:97645285 | C | A | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+61C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 5/22 | chr9 | 97645285 | |||||||
| chr9:97645294 | A | G | 2 | a0001c0002t0002g0047 a0001c0002t0002g0084 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.489+70A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 5/22 | chr9 | 97645294 | |||||||
| chr9:97645298 | C | T | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+74C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 5/22 | chr9 | 97645298 | |||||||
| chr9:97645845 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.611+113A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97645845 | |||||||
| chr9:97646063 | C | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.611+331C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646063 | |||||||
| chr9:97646068 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(63): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.611+336C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646068 | |||||||
| chr9:97646115 | C | T | 2 | a0001c0002t0002g0021 a0001c0002t0002g0083 |
3 | HG03225.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.611+383C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646115 | |||||||
| chr9:97646488 | C | T | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.611+756C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646488 | |||||||
| chr9:97646501 | C | G | 1 | a0001c0001t0001g0192 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.611+769C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646501 | |||||||
| chr9:97646558 | G | A | 26 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.611+826G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646558 | |||||||
| chr9:97646768 | C | T | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-724C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646768 | |||||||
| chr9:97646786 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.612-706G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646786 | |||||||
| chr9:97646839 | C | CA | 37 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0099 others(34): Show |
39 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.612-630dupA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 97646839 | ||||||
| chr9:97646839 | CA | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0191 a0001c0001t0001g0223 others(3): Show |
6 | HG00597.hp2 HG01192.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.612-630delA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 97646839 | ||||||
| chr9:97646839 | CAA | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00609.hp1 HG01099.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.612-631_612-630del others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 97646839 | ||||||
| chr9:97646839 | CAAA | C | 13 | a0001c0002t0005g0019 a0001c0002t0005g0065 a0001c0002t0005g0066 others(10): Show |
14 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.612-632_612-630del others(3): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 97646839 | ||||||
| chr9:97646839 | CAAAA | C | 27 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(24): Show |
33 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.612-633_612-630del others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 97646839 | ||||||
| chr9:97646934 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02809.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.612-558T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97646934 | |||||||
| chr9:97647009 | T | C | 2 | a0001c0002t0002g0021 a0001c0002t0002g0083 |
3 | HG03225.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.612-483T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97647009 | |||||||
| chr9:97647264 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.612-228T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97647264 | |||||||
| chr9:97647265 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.612-227T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 6/22 | chr9 | 97647265 | |||||||
| chr9:97647683 | G | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.681+122G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 7/22 | chr9 | 97647683 | |||||||
| chr9:97647705 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.681+144G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 7/22 | chr9 | 97647705 | |||||||
| chr9:97647821 | C | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.682-187C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 7/22 | chr9 | 97647821 | |||||||
| chr9:97647943 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.682-65A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 7/22 | chr9 | 97647943 | |||||||
| chr9:97648268 | T | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.897+45T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648268 | |||||||
| chr9:97648288 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.897+65G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648288 | |||||||
| chr9:97648442 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.897+219A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648442 | |||||||
| chr9:97648487 | G | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.897+264G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648487 | |||||||
| chr9:97648532 | T | C | 1 | a0001c0002t0018g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.897+309T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648532 | |||||||
| chr9:97648949 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.897+726G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648949 | |||||||
| chr9:97648965 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.897+742G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97648965 | |||||||
| chr9:97649344 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.897+1121C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649344 | |||||||
| chr9:97649455 | T | C | 1 | a0001c0002t0018g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.898-1048T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649455 | |||||||
| chr9:97649545 | T | C | 1 | a0001c0002t0013g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.898-958T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649545 | |||||||
| chr9:97649600 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.898-903A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649600 | |||||||
| chr9:97649627 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | NA19006.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.898-876A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649627 | |||||||
| chr9:97649652 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.898-851T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649652 | |||||||
| chr9:97649735 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.898-768G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97649735 | |||||||
| chr9:97649738 | A | AT | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(146): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.898-752dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 97649738 | ||||||
| chr9:97649738 | A | ATT | 26 | a0001c0001t0001g0114 a0001c0001t0001g0240 a0001c0001t0001g0274 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.898-753_898-752dup others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 97649738 | ||||||
| chr9:97650093 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0099 others(14): Show |
20 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.898-410C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650093 | |||||||
| chr9:97650219 | A | G | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.898-284A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650219 | |||||||
| chr9:97650234 | G | A | 1 | a0001c0001t0003g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.898-269G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650234 | |||||||
| chr9:97650344 | A | G | 1 | a0001c0002t0013g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.898-159A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650344 | |||||||
| chr9:97650369 | T | G | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.898-134T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650369 | |||||||
| chr9:97650422 | T | C | 1 | a0001c0002t0002g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.898-81T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650422 | |||||||
| chr9:97650479 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.898-24G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 8/22 | chr9 | 97650479 | |||||||
| chr9:97650683 | G | A | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.995+83G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | chr9 | 97650683 | |||||||
| chr9:97650785 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.995+185T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | chr9 | 97650785 | |||||||
| chr9:97650810 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.995+210G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | chr9 | 97650810 | |||||||
| chr9:97650816 | T | G | 1 | a0001c0001t0003g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.995+216T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | chr9 | 97650816 | |||||||
| chr9:97650931 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.995+331G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | chr9 | 97650931 | |||||||
| chr9:97650939 | A | ATT | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.995+349_995+350dup others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr9 | 97650939 | ||||||
| chr9:97651602 | A | T | 2 | a0001c0001t0003g0190 a0001c0001t0003g0207 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1059+229A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97651602 | |||||||
| chr9:97651657 | A | T | 1 | a0001c0002t0002g0059 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1059+284A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97651657 | |||||||
| chr9:97651733 | TAGAC | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1059+364_1059+367d others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97651733 | ||||||
| chr9:97651837 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1059+464A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97651837 | |||||||
| chr9:97651925 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1059+552T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97651925 | |||||||
| chr9:97652008 | AT | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1059+647delT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97652008 | ||||||
| chr9:97652095 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1059+722C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652095 | |||||||
| chr9:97652148 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1059+775T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652148 | |||||||
| chr9:97652204 | A | G | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1059+831A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652204 | |||||||
| chr9:97652334 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1059+961T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652334 | |||||||
| chr9:97652360 | A | G | 1 | a0001c0008t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+987A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652360 | |||||||
| chr9:97652473 | A | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1059+1100A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652473 | |||||||
| chr9:97652651 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1060-1147A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652651 | |||||||
| chr9:97652891 | G | A | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1060-907G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652891 | |||||||
| chr9:97652896 | G | A | 6 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0083 others(3): Show |
8 | HG01891.hp1 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060-902G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652896 | |||||||
| chr9:97652993 | A | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1060-805A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97652993 | |||||||
| chr9:97653047 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1060-751A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653047 | |||||||
| chr9:97653119 | C | CT | 6 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0239 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-660dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97653119 | ||||||
| chr9:97653119 | C | CTT | 18 | a0001c0002t0002g0080 a0001c0002t0002g0081 a0001c0002t0005g0019 others(15): Show |
19 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-661_1060-660d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97653119 | ||||||
| chr9:97653119 | C | CTTT | 17 | a0001c0002t0002g0047 a0001c0002t0002g0084 a0001c0003t0004g0009 others(14): Show |
21 | HG01952.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1060-662_1060-660d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97653119 | ||||||
| chr9:97653119 | C | CTTTT | 7 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0046 others(4): Show |
9 | HG01167.hp1 HG01891.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-663_1060-660d others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97653119 | ||||||
| chr9:97653119 | C | CTTTTT | 18 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(15): Show |
31 | HG00609.hp1 HG01099.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1060-664_1060-660d others(7): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr9 | 97653119 | ||||||
| chr9:97653202 | C | A | 1 | a0001c0002t0017g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-596C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653202 | |||||||
| chr9:97653206 | C | T | 1 | a0001c0005t0006g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1060-592C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653206 | |||||||
| chr9:97653441 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1060-357A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653441 | |||||||
| chr9:97653558 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(187): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1060-240G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653558 | |||||||
| chr9:97653575 | G | A | 16 | a0001c0002t0002g0047 a0001c0002t0002g0084 a0001c0002t0005g0019 others(13): Show |
17 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-223G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653575 | |||||||
| chr9:97653675 | AAG | A | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1060-122_1060-121d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 10/22 | chr9 | 97653675 | |||||||
| chr9:97654018 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0001g0154 others(2): Show |
6 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+110A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654018 | |||||||
| chr9:97654317 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(125): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1170+409G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654317 | |||||||
| chr9:97654390 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1170+482G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654390 | |||||||
| chr9:97654448 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1171-432C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654448 | |||||||
| chr9:97654564 | T | TA | 30 | a0001c0002t0002g0021 a0001c0002t0002g0047 a0001c0002t0002g0083 others(27): Show |
36 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1171-302dupA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 97654564 | ||||||
| chr9:97654564 | TA | T | 6 | a0001c0001t0001g0216 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG02135.hp1 NA18951.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1171-302delA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 97654564 | ||||||
| chr9:97654576 | AAAG | A | 19 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(16): Show |
32 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1171-300_1171-298d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 97654576 | ||||||
| chr9:97654596 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1171-284G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654596 | |||||||
| chr9:97654619 | G | C | 14 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0140 others(11): Show |
16 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1171-261G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 11/22 | chr9 | 97654619 | |||||||
| chr9:97655014 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1235+70A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655014 | |||||||
| chr9:97655045 | G | GT | 61 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(58): Show |
81 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.1235+108dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 97655045 | ||||||
| chr9:97655100 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1235+156T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655100 | |||||||
| chr9:97655110 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1235+166C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655110 | |||||||
| chr9:97655212 | A | G | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1235+268A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655212 | |||||||
| chr9:97655258 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1235+314T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655258 | |||||||
| chr9:97655393 | A | AT | 26 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1236-309_1236-308i others(3): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655393 | |||||||
| chr9:97655394 | A | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1236-308A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655394 | |||||||
| chr9:97655433 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1236-269T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655433 | |||||||
| chr9:97655606 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1236-96G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 12/22 | chr9 | 97655606 | |||||||
| chr9:97656151 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1373+66T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656151 | |||||||
| chr9:97656505 | G | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1373+420G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656505 | |||||||
| chr9:97656547 | A | T | 3 | a0002c0006t0001g0244 a0002c0006t0001g0263 a0002c0006t0001g0264 |
3 | HG01167.hp2 HG01168.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1373+462A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656547 | |||||||
| chr9:97656712 | C | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0005t0006g0017 others(3): Show |
8 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1373+627C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656712 | |||||||
| chr9:97656915 | G | C | 2 | a0001c0002t0002g0088 a0003c0009t0002g0087 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1373+830G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656915 | |||||||
| chr9:97656922 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1373+837G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97656922 | |||||||
| chr9:97657132 | A | C | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1373+1047A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657132 | |||||||
| chr9:97657202 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1373+1117G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657202 | |||||||
| chr9:97657239 | T | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(62): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1373+1154T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657239 | |||||||
| chr9:97657327 | T | C | 12 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1373+1242T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657327 | |||||||
| chr9:97657505 | C | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1374-1135C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657505 | |||||||
| chr9:97657581 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1374-1059A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657581 | |||||||
| chr9:97657623 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1374-1017C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657623 | |||||||
| chr9:97657662 | A | AT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0001g0154 others(2): Show |
6 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1374-978_1374-977i others(3): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657662 | |||||||
| chr9:97657860 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(247): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1374-780G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657860 | |||||||
| chr9:97657880 | G | A | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1374-760G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657880 | |||||||
| chr9:97657885 | G | GCT | 12 | a0001c0001t0001g0142 a0001c0001t0001g0196 a0001c0001t0001g0241 others(9): Show |
14 | HG00544.hp2 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1374-734_1374-733d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657885 | ||||||
| chr9:97657885 | G | GCTCTCTC others(1): Show |
11 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(8): Show |
12 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1374-740_1374-733d others(10): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657885 | ||||||
| chr9:97657885 | G | GCTCTCTC others(3): Show |
1 | a0001c0002t0005g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1374-742_1374-733d others(12): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657885 | ||||||
| chr9:97657885 | G | GCTCTCTC others(5): Show |
5 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374-744_1374-733d others(14): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657885 | ||||||
| chr9:97657887 | T | G | 3 | a0001c0001t0003g0220 a0001c0002t0002g0080 a0001c0002t0002g0081 |
3 | HG02630.hp2 HG02886.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1374-753T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657887 | |||||||
| chr9:97657906 | C | A | 11 | a0001c0001t0001g0107 a0001c0001t0001g0118 a0001c0001t0001g0121 others(8): Show |
12 | HG00099.hp2 HG01891.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1374-734C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657906 | |||||||
| chr9:97657906 | C | CTCTA | 3 | a0001c0001t0001g0042 a0001c0001t0001g0246 a0001c0001t0001g0262 |
4 | NA18949.hp1 NA18955.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1374-733_1374-732i others(6): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657906 | ||||||
| chr9:97657906 | CTA | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0034 others(41): Show |
48 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1374-714_1374-713d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657906 | ||||||
| chr9:97657908 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1374-732A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657908 | |||||||
| chr9:97657910 | A | C | 117 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0033 others(114): Show |
141 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1374-730A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657910 | |||||||
| chr9:97657912 | A | C | 55 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0035 others(52): Show |
72 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1374-728A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657912 | |||||||
| chr9:97657914 | A | C | 9 | a0001c0001t0003g0097 a0001c0002t0002g0061 a0001c0002t0005g0019 others(6): Show |
10 | HG01884.hp1 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1374-726A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657914 | |||||||
| chr9:97657916 | A | C | 3 | a0001c0002t0005g0065 a0001c0002t0005g0068 a0001c0002t0005g0072 |
3 | HG03471.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1374-724A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657916 | |||||||
| chr9:97657921 | TATA | T | 1 | a0001c0001t0001g0010 | 3 | HG02698.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1374-718_1374-716d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657921 | |||||||
| chr9:97657923 | TATA | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0247 a0001c0001t0001g0251 others(2): Show |
5 | HG01978.hp2 HG03098.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374-716_1374-714d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657923 | |||||||
| chr9:97657924 | A | AT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0258 a0001c0001t0001g0274 others(1): Show |
4 | HG01361.hp1 HG02040.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374-715dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657924 | ||||||
| chr9:97657924 | A | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | NA19006.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1374-716A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657924 | |||||||
| chr9:97657924 | ATAT | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0028 others(18): Show |
23 | HG00438.hp2 HG00673.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.1374-714_1374-712d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657924 | ||||||
| chr9:97657925 | TA | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0174 a0001c0005t0006g0275 |
3 | HG01081.hp1 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1374-714delA | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657925 | |||||||
| chr9:97657926 | A | AT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(19): Show |
30 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1374-697dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657926 | ||||||
| chr9:97657926 | A | ATAT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0243 a0001c0001t0001g0245 others(5): Show |
8 | HG00597.hp1 HG01106.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1374-713_1374-712i others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657926 | ||||||
| chr9:97657926 | A | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0157 others(9): Show |
14 | HG01361.hp1 HG01361.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1374-714A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657926 | |||||||
| chr9:97657926 | AT | A | 51 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0025 others(48): Show |
58 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1374-697delT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657926 | ||||||
| chr9:97657926 | ATT | A | 23 | a0001c0001t0001g0103 a0001c0001t0001g0147 a0001c0001t0001g0179 others(20): Show |
27 | HG01496.hp2 HG01891.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.1374-698_1374-697d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657926 | ||||||
| chr9:97657926 | ATTT | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
12 | HG00741.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1374-699_1374-697d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 97657926 | ||||||
| chr9:97657927 | T | TA | 9 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0164 others(6): Show |
9 | HG00597.hp2 HG01981.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1374-713_1374-712i others(3): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657927 | |||||||
| chr9:97657927 | T | TATA | 2 | a0001c0001t0001g0043 a0001c0001t0001g0173 |
3 | HG02056.hp1 NA19003.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1374-713_1374-712i others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657927 | |||||||
| chr9:97657928 | T | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(40): Show |
59 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1374-712T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657928 | |||||||
| chr9:97657929 | T | A | 28 | a0001c0001t0001g0100 a0001c0001t0001g0126 a0001c0001t0001g0128 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374-711T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657929 | |||||||
| chr9:97657930 | T | A | 15 | a0001c0001t0001g0203 a0001c0001t0003g0199 a0001c0002t0002g0088 others(12): Show |
19 | HG00621.hp1 HG01952.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1374-710T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657930 | |||||||
| chr9:97657931 | T | A | 18 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(15): Show |
19 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1374-709T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657931 | |||||||
| chr9:97657932 | T | A | 3 | a0001c0002t0002g0088 a0001c0002t0017g0062 a0003c0009t0002g0087 |
3 | HG02145.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1374-708T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657932 | |||||||
| chr9:97657933 | T | A | 18 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(15): Show |
19 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1374-707T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657933 | |||||||
| chr9:97657934 | T | A | 1 | a0001c0002t0017g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1374-706T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657934 | |||||||
| chr9:97657935 | T | A | 13 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(10): Show |
14 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1374-705T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657935 | |||||||
| chr9:97657953 | AG | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0104 a0001c0001t0001g0109 |
4 | HG00642.hp1 HG01255.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374-686delG | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657953 | |||||||
| chr9:97657990 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1374-650C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657990 | |||||||
| chr9:97657991 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1374-649A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97657991 | |||||||
| chr9:97658054 | C | T | 2 | a0001c0001t0003g0199 a0001c0001t0003g0226 |
2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1374-586C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658054 | |||||||
| chr9:97658141 | T | C | 4 | a0001c0005t0006g0017 a0001c0005t0006g0112 a0001c0005t0006g0228 others(1): Show |
6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1374-499T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658141 | |||||||
| chr9:97658163 | AC | A | 12 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1374-476delC | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658163 | |||||||
| chr9:97658257 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1374-383C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658257 | |||||||
| chr9:97658276 | C | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1374-364C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658276 | |||||||
| chr9:97658307 | T | C | 26 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1374-333T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658307 | |||||||
| chr9:97658426 | C | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0208 |
3 | NA18940.hp1 NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1374-214C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658426 | |||||||
| chr9:97658427 | C | G | 1 | a0001c0002t0018g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374-213C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658427 | |||||||
| chr9:97658577 | C | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1374-63C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 14/22 | chr9 | 97658577 | |||||||
| chr9:97658851 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1477+108A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97658851 | |||||||
| chr9:97659014 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1477+271C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659014 | |||||||
| chr9:97659026 | C | T | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1477+283C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659026 | |||||||
| chr9:97659405 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1477+662T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659405 | |||||||
| chr9:97659471 | G | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1477+728G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659471 | |||||||
| chr9:97659487 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0182 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1477+744G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659487 | |||||||
| chr9:97659599 | G | A | 7 | a0001c0002t0002g0008 a0001c0002t0002g0048 a0001c0002t0002g0049 others(4): Show |
9 | HG00609.hp1 NA18962.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1477+856G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659599 | |||||||
| chr9:97659745 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(187): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1477+1002G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659745 | |||||||
| chr9:97659786 | T | G | 1 | a0001c0002t0002g0007 | 3 | NA18966.hp2 NA19002.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1477+1043T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659786 | |||||||
| chr9:97659793 | T | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00099.hp2 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1477+1050T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659793 | |||||||
| chr9:97659800 | G | T | 58 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(55): Show |
76 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(73): Show |
intron_variant | MODIFIER | c.1477+1057G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97659800 | |||||||
| chr9:97660044 | G | T | 58 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(55): Show |
76 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(73): Show |
intron_variant | MODIFIER | c.1478-902G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97660044 | |||||||
| chr9:97660208 | G | A | 3 | a0001c0001t0003g0141 a0001c0003t0004g0020 a0001c0003t0004g0079 |
4 | HG02976.hp2 HG03579.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1478-738G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97660208 | |||||||
| chr9:97660311 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1478-635C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97660311 | |||||||
| chr9:97660656 | A | C | 1 | a0001c0008t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1478-290A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97660656 | |||||||
| chr9:97660908 | T | G | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-38T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 15/22 | chr9 | 97660908 | |||||||
| chr9:97661631 | T | C | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1601-411T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | chr9 | 97661631 | |||||||
| chr9:97661732 | G | GT | 66 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0033 others(63): Show |
72 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1601-292dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 97661732 | ||||||
| chr9:97661732 | GT | G | 28 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(25): Show |
30 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1601-292delT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 97661732 | ||||||
| chr9:97661732 | GTT | G | 52 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0002t0002g0001 others(49): Show |
71 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(68): Show |
intron_variant | MODIFIER | c.1601-293_1601-292d others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 97661732 | ||||||
| chr9:97661732 | GTTT | G | 8 | a0001c0003t0004g0009 a0001c0003t0004g0022 a0001c0003t0004g0089 others(5): Show |
11 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1601-294_1601-292d others(5): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 97661732 | ||||||
| chr9:97661737 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1601-305T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | chr9 | 97661737 | |||||||
| chr9:97661793 | A | AT | 75 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0027 others(72): Show |
99 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1601-238dupT | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 97661793 | ||||||
| chr9:97661930 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1601-112T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | chr9 | 97661930 | |||||||
| chr9:97661941 | C | T | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1601-101C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | chr9 | 97661941 | |||||||
| chr9:97661973 | C | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1601-69C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 16/22 | chr9 | 97661973 | |||||||
| chr9:97662208 | T | C | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1703+64T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662208 | |||||||
| chr9:97662291 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1703+147G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662291 | |||||||
| chr9:97662345 | A | G | 1 | a0001c0004t0012g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1703+201A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662345 | |||||||
| chr9:97662352 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1703+208G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662352 | |||||||
| chr9:97662399 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1703+255G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662399 | |||||||
| chr9:97662502 | A | G | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1703+358A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662502 | |||||||
| chr9:97662567 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0266 |
2 | HG00408.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1704-387A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662567 | |||||||
| chr9:97662836 | A | G | 1 | a0001c0002t0002g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1704-118A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 17/22 | chr9 | 97662836 | |||||||
| chr9:97663058 | T | C | 2 | a0001c0002t0002g0047 a0001c0002t0002g0084 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1797+11T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663058 | |||||||
| chr9:97663100 | A | T | 1 | a0001c0001t0003g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1797+53A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663100 | |||||||
| chr9:97663412 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1797+365A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663412 | |||||||
| chr9:97663470 | C | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1797+423C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663470 | |||||||
| chr9:97663477 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1797+430G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663477 | |||||||
| chr9:97663593 | C | T | 2 | a0001c0002t0017g0062 a0001c0002t0018g0082 |
2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1797+546C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663593 | |||||||
| chr9:97663700 | G | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1798-640G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663700 | |||||||
| chr9:97663736 | C | T | 1 | a0001c0002t0002g0018 | 2 | NA18947.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1798-604C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663736 | |||||||
| chr9:97663778 | G | T | 5 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0083 others(2): Show |
7 | HG01891.hp1 HG02976.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1798-562G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663778 | |||||||
| chr9:97663929 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1798-411A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97663929 | |||||||
| chr9:97664008 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0183 |
2 | HG01361.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1798-332G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97664008 | |||||||
| chr9:97664134 | G | A | 1 | a0001c0004t0012g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1798-206G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97664134 | |||||||
| chr9:97664194 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1798-146T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97664194 | |||||||
| chr9:97664289 | ATG | A | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1798-43_1798-42del others(2): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 97664289 | ||||||
| chr9:97664325 | A | G | 2 | a0001c0001t0001g0189 a0001c0002t0002g0088 |
2 | NA18956.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1798-15A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 18/22 | chr9 | 97664325 | |||||||
| chr9:97664541 | A | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1901+98A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664541 | |||||||
| chr9:97664574 | T | C | 1 | a0001c0002t0002g0006 | 3 | HG01099.hp2 HG01192.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1901+131T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664574 | |||||||
| chr9:97664580 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1901+137A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664580 | |||||||
| chr9:97664667 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1901+224G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664667 | |||||||
| chr9:97664787 | C | G | 26 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
39 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1901+344C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664787 | |||||||
| chr9:97664808 | G | C | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1901+365G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664808 | |||||||
| chr9:97664981 | C | T | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901+538C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97664981 | |||||||
| chr9:97665119 | A | G | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901+676A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665119 | |||||||
| chr9:97665191 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0016g0105 |
2 | HG01496.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1901+748A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665191 | |||||||
| chr9:97665275 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1901+832C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665275 | |||||||
| chr9:97665291 | C | G | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1901+848C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665291 | |||||||
| chr9:97665348 | C | T | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1901+905C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665348 | |||||||
| chr9:97665395 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1901+952C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665395 | |||||||
| chr9:97665426 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1901+983C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665426 | |||||||
| chr9:97665528 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0286 |
2 | NA18943.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1901+1085C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665528 | |||||||
| chr9:97665582 | G | A | 2 | a0001c0002t0002g0047 a0001c0002t0002g0084 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1901+1139G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665582 | |||||||
| chr9:97665742 | C | G | 1 | a0001c0003t0004g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1902-1021C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665742 | |||||||
| chr9:97665765 | C | A | 1 | a0001c0003t0004g0020 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1902-998C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665765 | |||||||
| chr9:97665855 | G | A | 1 | a0001c0001t0010g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1902-908G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97665855 | |||||||
| chr9:97666009 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1902-754G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666009 | |||||||
| chr9:97666098 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1902-665C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666098 | |||||||
| chr9:97666346 | A | G | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1902-417A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666346 | |||||||
| chr9:97666409 | T | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1902-354T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666409 | |||||||
| chr9:97666502 | G | T | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1902-261G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666502 | |||||||
| chr9:97666537 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1902-226G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666537 | |||||||
| chr9:97666551 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.1902-212G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666551 | |||||||
| chr9:97666607 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1902-156A>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666607 | |||||||
| chr9:97666695 | A | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0099 others(14): Show |
20 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1902-68A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 19/22 | chr9 | 97666695 | |||||||
| chr9:97666897 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2016+20G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97666897 | |||||||
| chr9:97666999 | A | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0180 others(1): Show |
4 | NA18983.hp2 NA19011.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2016+122A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97666999 | |||||||
| chr9:97667083 | G | T | 1 | a0001c0008t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2016+206G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667083 | |||||||
| chr9:97667127 | A | C | 1 | a0001c0001t0001g0010 | 3 | HG02698.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2016+250A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667127 | |||||||
| chr9:97667146 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2016+269G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667146 | |||||||
| chr9:97667193 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.2016+316G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667193 | |||||||
| chr9:97667238 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2016+361A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667238 | |||||||
| chr9:97667278 | C | T | 2 | a0001c0003t0004g0020 a0001c0003t0004g0079 |
3 | HG02976.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2016+401C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667278 | |||||||
| chr9:97667394 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2016+517T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667394 | |||||||
| chr9:97667397 | A | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2016+520A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667397 | |||||||
| chr9:97667418 | G | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0099 others(14): Show |
20 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.2016+541G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667418 | |||||||
| chr9:97667438 | G | A | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2016+561G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667438 | |||||||
| chr9:97667456 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2016+579G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667456 | |||||||
| chr9:97667694 | C | G | 1 | a0001c0004t0007g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2016+817C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667694 | |||||||
| chr9:97667948 | G | A | 1 | a0001c0001t0010g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2017-898G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667948 | |||||||
| chr9:97667993 | G | C | 4 | a0001c0005t0006g0017 a0001c0005t0006g0112 a0001c0005t0006g0228 others(1): Show |
6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-853G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97667993 | |||||||
| chr9:97668009 | T | C | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2017-837T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668009 | |||||||
| chr9:97668113 | C | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0005t0006g0017 others(3): Show |
8 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2017-733C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668113 | |||||||
| chr9:97668473 | G | C | 1 | a0001c0001t0001g0287 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2017-373G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668473 | |||||||
| chr9:97668541 | C | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG02135.hp1 NA18954.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017-305C>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668541 | |||||||
| chr9:97668639 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2017-207A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668639 | |||||||
| chr9:97668640 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(124): Show |
160 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.2017-206T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668640 | |||||||
| chr9:97668689 | G | A | 1 | a0001c0002t0013g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2017-157G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668689 | |||||||
| chr9:97668711 | G | A | 65 | a0001c0001t0001g0034 a0001c0001t0001g0144 a0001c0001t0001g0167 others(62): Show |
86 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(83): Show |
intron_variant | MODIFIER | c.2017-135G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668711 | |||||||
| chr9:97668715 | TG | T | 39 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(36): Show |
50 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2017-124delG | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr9 | 97668715 | ||||||
| chr9:97668716 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2017-130G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668716 | |||||||
| chr9:97668734 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2017-112T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668734 | |||||||
| chr9:97668827 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2017-19G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 20/22 | chr9 | 97668827 | |||||||
| chr9:97669030 | T | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2145+56T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669030 | |||||||
| chr9:97669171 | A | C | 6 | a0001c0004t0007g0074 a0001c0004t0007g0075 a0001c0004t0007g0076 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2145+197A>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669171 | |||||||
| chr9:97669188 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0183 |
2 | HG01361.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2145+214G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669188 | |||||||
| chr9:97669267 | T | C | 1 | a0001c0002t0018g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2145+293T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669267 | |||||||
| chr9:97669290 | T | C | 36 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0047 others(33): Show |
43 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.2146-303T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669290 | |||||||
| chr9:97669438 | C | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.2146-155C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 21/22 | chr9 | 97669438 | |||||||
| chr9:97669850 | C | G | 79 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0099 others(76): Show |
102 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.2259+144C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97669850 | |||||||
| chr9:97669912 | C | G | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2259+206C>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97669912 | |||||||
| chr9:97669915 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2259+209A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97669915 | |||||||
| chr9:97670099 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2259+393T>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670099 | |||||||
| chr9:97670197 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2259+491C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670197 | |||||||
| chr9:97670226 | G | A | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(37): Show |
51 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2259+520G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670226 | |||||||
| chr9:97670300 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0109 |
3 | HG00642.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2259+594G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670300 | |||||||
| chr9:97670303 | T | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2259+597T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670303 | |||||||
| chr9:97670378 | G | A | 61 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(58): Show |
81 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.2259+672G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670378 | |||||||
| chr9:97670509 | A | G | 1 | a0001c0002t0002g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2260-577A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670509 | |||||||
| chr9:97670536 | C | CGA | 11 | a0001c0003t0004g0009 a0001c0003t0004g0020 a0001c0003t0004g0022 others(8): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2260-550_2260-549i others(4): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670536 | |||||||
| chr9:97670619 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2260-467T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670619 | |||||||
| chr9:97670711 | G | T | 20 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(17): Show |
33 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2260-375G>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670711 | |||||||
| chr9:97670715 | G | C | 12 | a0001c0002t0005g0019 a0001c0002t0005g0063 a0001c0002t0005g0064 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2260-371G>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670715 | |||||||
| chr9:97670716 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2260-370T>C | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670716 | |||||||
| chr9:97670782 | G | A | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.2260-304G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670782 | |||||||
| chr9:97670785 | C | T | 62 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0007 others(59): Show |
82 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.2260-301C>T | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670785 | |||||||
| chr9:97670951 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(187): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2260-135G>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670951 | |||||||
| chr9:97670986 | T | A | 2 | a0001c0002t0002g0088 a0003c0009t0002g0087 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2260-100T>A | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97670986 | |||||||
| chr9:97671041 | A | G | 1 | a0001c0002t0017g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2260-45A>G | NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 22/22 | chr9 | 97671041 |